Product Name Or Brand
Start broad with the product name, manufacturer, retailer brand or model family. This is usually the fastest way to find a possible notice.
Start with the product name or brand. If the list is too broad, search the exact UPC, lot code, model number, date code, NHTSA campaign number or official recall number printed on the notice or label.
Results help you find a possible match quickly. Before you stop use, discard, return or repair anything, open the official notice and confirm every affected detail.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
Mikario Trading Convertible Baby Gyms Recalled Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standard for Infant Support Cushions; Sold on TikTok Shop
This recall involves Mikario Trading's 5-in-1 baby gyms. The recalled baby gyms convert from an activity center to a tummy-time pillow mat. They were sold in pink and have a toy bar, six detachable plush toys and a set of milestone cards. "Baby Gym" and "Item No.: CBPBG-PIN" are printed on a label stitched to the product on the edge of the mat at the bottom.
|
CPSC
10577
|
Child/Baby | High |
Jan 22, 2026
Recall: Jan 22, 2026
|
Details |
Johnson Health Tech Expands Recall to Include Matrix Retail and Vision Treadmills Due to Fire Hazard
This recall involves Matrix Retail models T30, TF30, T50, TF50, and T75 treadmills, and Vision models T9800, TF20, T40, and T80 treadmills with certain serial numbers. The treadmills have a running platform that measures 60 inches long by 20 inches wide, a 33-inch-wide console, and were sold with a straight power cord with no power cord bracket. "Matrix" or "Vision" is printed on the treadmill and treadmill belt. The model number and frame serial number are located on the lower front crossbar near the power switch. The serial number includes the letters TM, a three-digit model number, and the manufacture date in YY/MM format followed by a five-digit serial. The recalled treadmills were manufactured from June 2007 through January 2024 and do not come with a power cord bracket. This recall is an expansion of the prior recall of Matrix T1 and T3 Series Commercial Treadmills, which were also recalled because the power cord can become loose from the treadmill's power socket. The remedy in the prior recall of commercial treadmills is a power cord bracket that requires tools for installation. For this recall expansion, the remedy for consumers is a power cord with an automatic locking-style plug that does not require any tools for installation. Model Name/ Number Recalled Serial Number(s) or Range Matrix Retail T30 (TM729) TM7291709CA00001 - TM7292104C00380 TF30 (TM693, TM693B) TM6931606CA00001 - TM6931705CA00178 TM693B1707CA00001 - TM693B2201C00601 T50 (TM695, TM767) TM6951607CA00001 - TM6952009C00840 TM7672009C00001 - TM76722011C00051 TF50 (TM694, TM694B, TM768) TM6941607CA00001 - TM69482009C00514 TM694B1605C00008 - TM694B2009K03263 TM7682009C00001 - TM7682104C00580 T75 (TM703, TM703B, TM703C, TM703E) TM7031607CA00001 - TM70381903C00088 TM70382311C00229 TM703B1609CA00015 - TM703B1908C00050 TM703B2309C00164, TM703B2311C00282 TM703C1810C00001 - TM703C2212C00127 TM703C2305C00049, TM703C2308C00409 TM703E2304C00002 - TM703E2401C00087 Vision T9800 (TM87) TM87D070600070, TM87D080600128, TM87D0940059, TM87D120100125, and TM87D1206000127 TF20 (TM432, TM432C) TM4321108BD00255 - TM4321610CA00033 TM432C1210CA00002 - TM432C1606CA00200 T40 (TM433, TM433C) TM4331201BD00466 - TM4331510BD00004 TM433C1408CJ00001 - TM433C1602CA00631 T80 (TM445) TM4451210BC00001 - TM4451505BC00150 TM4451212BD00002 - TM4451406BD00125
|
CPSC
10569
|
Consumer Product | Unknown |
Jan 22, 2026
Recall: Jan 22, 2026
|
Details |
Iristar Minoxidil Spray Bottles for Hair and Beard Growth Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Moralowen
This recall involves Iristar Minoxidil Spray Bottles, 5% minoxidil with biotin for hair and beard growth. The sprays come in black plastic bottles with navy blue labels and white highlights with a spray cap. The bottles and outer packaging are labeled "Iristar" and "Minoxidil Spray" on the front and ingredients and directions for use are found on the back.
|
CPSC
10576
|
Child/Baby | High |
Jan 22, 2026
Recall: Jan 22, 2026
|
Details |
Gagaku Children's Ice Cream Toy Playsets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion Hazard; Violate Mandatory Standard for Toys; Sold on Amazon by Brandworl.USA
This recall involves Gagaku-branded ice cream shop toy playsets. The recalled toy set includes 16 wooden pieces: a cash register, three ice cream cones, six scoops of ice cream, four popsicles, and two cupcakes in varying colors or "flavors." It also comes with one plastic credit card, five plastic dollar bills, one plastic menu and a two-level pink display box labeled "ICE-CREAM" on the front, with a black sign on the side. "GAGAKU" and "Model: KABI-0176 G062401IC" are printed on a label on the underside of the toy.
|
CPSC
10571
|
Child/Baby | High |
Jan 22, 2026
Recall: Jan 22, 2026
|
Details |
Based Online Fidget Magnet Ball Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys
This recall involves Based Online Fidget Magnet Ball Toy Sets. Each set includes four textured, silicone-covered magnet balls in white, yellow, blue and purple. Each ball is about 1.24 inches in diameter. The magnet toys come in a black fabric zippered case. There are no identifying marks on the magnet toys.
|
CPSC
10573
|
Child/Baby | High |
Jan 22, 2026
Recall: Jan 22, 2026
|
Details |
Academy Sports + Outdoors Recalls Magellan Odyssey Rocker Chairs Due to Injury and Fall Hazards
This recall involves Academy Sports + Outdoors' Magellan-branded Odyssey Rocker Chairs with date codes 07/2025 or 08/2025 sold from September 2025 to October 2025. The recalled folding chairs were sold in charcoal, navy, olive green and teal and measure about 25.2" long by 5.5" deep by 37.4" high when folded or 25.4" long by 25.2" deep by 37.4" high when opened. They have a metal frame with a mesh backrest, a carrying handle and a drink holder on the side. The Magellan Outdoors logo is printed on the front of the backrest. Only chairs manufactured between July 2025 through August 2025 are included in this recall. "ACADEMY, LTD," "177296" and the manufacture date in MM/YYYY format are printed on the tracking label sewn onto the seat of the chair.
|
CPSC
10568
|
Consumer Product | Medium |
Jan 22, 2026
Recall: Jan 22, 2026
|
Details |
Aborder Products Recalls Cumbor Retractable Safety Gates Due to Risk of Serious Injury or Death to Children from Entrapment; Violates Mandatory Standard for Gates and Enclosures
This recall involves Cumbor-branded retractable safety gates. The recalled gates have a metal frame and a mesh screen that measures about 34 inches high with an adjustable width up to 55 inches. The gates were sold in black, gray, and white and came with one or more suction cups. "Model Name: Retractable Safety Gate," "Model Number: S5V2" and "Cohort Information: A202504S5V2A001" are printed on a label sewn to the mesh screen.
|
CPSC
10575
|
Child/Baby | High |
Jan 22, 2026
Recall: Jan 22, 2026
|
Details |
|
Medline medical procedure convenience kits labeled as: 1) ROBOTIC, REF CDS980523M; 2) ROBOTIC GYN, REF CDS980647K; 3) DAVINCI PROCEDURE, REF CDS980864Q; 4) GYN-URO LAPSCP CDS-LF, REF CDS981583U; 5) GYN-URO LAPSCP CDS-LF, REF CDS981583V; 6) GYN ROBOTIC, REF CDS981826K; 7) DEPAUL DAVINCI CDS, REF CDS982377K; 8) GU DAVINCI, REF CDS982779N; 9) GYN DAVINCI, REF CDS982780V; 10) UNIVERSAL ROBOTIC ORLANDO, REF CDS982857K; 11) ROBOTIC GU/GYN, REF CDS983393L; 12) GYN LAPAROSCOPY CDS, REF CDS984656Q; 13) GYN LAPAROSCOPY CDS, REF CDS984656R; 14) DAVINCI CDS UCC-LF, REF CDS984663J; 15) ROBOTIC UROLOGY PROS
Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) during use.
|
FDA
Z-1088-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Dec 16, 2025
|
Details |
|
Allura Xper FD20; Model Number: 722006;
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.
|
FDA
Z-1066-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Dec 15, 2025
|
Details |
|
Allura Xper FD10; Model Number: 722026;
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.
|
FDA
Z-1073-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Dec 15, 2025
|
Details |
|
FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
|
FDA
Z-1023-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Nov 24, 2025
|
Details |
|
Brand Name: PALACOS Product Name: PALACOS MV+G pro 40; PALACOS MV+G pro 80 Model/Catalog Number: 5081290; 5081291 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix). Component: N/A
increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.
|
FDA
Z-1082-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Dec 9, 2025
|
Details |
|
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) OPEN HEART ACCESSORY CDSKit SKU CDS984289O; 2) OPEN HEART CDSKit SKU CDS984355K; 3) BAG A OPEN HEART KITKit SKU DYKM1025D; 4) RR-CABG SUPPLEMENTAL PACKKit SKU DYNJ0394752O; 5) OPEN HEART CDSKit SKU DYNJ902879T; 6) BASIC CARDIAC ANESTHESIAKit SKU DYNJ903523F; 7) OPEN HEART CDSKit SKU DYNJ905557B; 8) AN03 HEART/ANESTHESIA KIT-LFKit SKU PHS972012D.
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.
|
FDA
Z-1050-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Nov 26, 2025
|
Details |
|
FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
|
FDA
Z-1022-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Nov 24, 2025
|
Details |
|
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) RR-LE FORT MANDIBLE PACK-LF, Medline Kit SKU DYNJ0785864R; 2) RR-ASC EAR PACK-LF, Medline Kit SKU DYNJ0792607R.
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.
|
FDA
Z-1052-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Nov 26, 2025
|
Details |
|
MAXXUS, System, Tomography, Computed, Emission
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affected Product Details section of this letter) could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury. There have been no reports of detector falls or injuries as a result of this potential issue. The Impacted Systems affected by this notice are those that have not been manufactured for several years. GE HealthCare has previously communicated End of Guaranteed Service for these Impacted Systems.
|
FDA
Z-1047-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Dec 10, 2025
|
Details |
|
Brand Name: PALACOS Product Name: PALACOS R pro 40; PALACOS R pro 80 Model/Catalog Number: 5081286; 5081287 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix). Component: N/A
increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.
|
FDA
Z-1080-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Dec 9, 2025
|
Details |
|
Brand Name: Catalyst+ Product Name: Catalyst, Catalyst+ Model/Catalog Number: SP001-0026, SP003-0002 Software Version: cSRS module in combination with cMotion module Product Description: GMDN: 40893 Patient positioning device, diagnostic imaging/radiotherapy, laser Component: Not applicable
Due to issues with the system's stereotactic radiosurgery (SRS) treatment cannot be guaranteed for all couch angles and system setups. n certain cases, the system may indicate the patient as correctly positioned at the isocenter, even when the isocenter is positioned outside of the indicated tolerance.
|
FDA
Z-1092-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Oct 9, 2025
|
Details |
|
Allura Xper FD20 Biplane; Model Number: 722013;
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.
|
FDA
Z-1071-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Dec 15, 2025
|
Details |
|
Allura Xper FD20 OR Table; Model Number: 722023;
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.
|
FDA
Z-1072-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Dec 15, 2025
|
Details |
|
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: RR-LAP DONOR NEP ACCESSORY, Medline kit SKU DYNJ63395B
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.
|
FDA
Z-1053-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Nov 26, 2025
|
Details |
|
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) IV START KIT NS, Medline kit SKU DYKM1980C; 2) (134) L&D IV-START SET, Medline kit SKU DYKM2137B; 3) IV START KIT, Medline kit SKU DYKS1372C; 4) IV START KIT, Medline kit SKU DYNDV1691B; 5) OUTPATIENT 2 TO 5 YEARS, Medline kit SKU DYNDV2464A.
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.
|
FDA
Z-1056-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Nov 26, 2025
|
Details |
|
SMV DSX New Line, System, Tomography, Computed, Emission
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affected Product Details section of this letter) could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury. There have been no reports of detector falls or injuries as a result of this potential issue. The Impacted Systems affected by this notice are those that have not been manufactured for several years. GE HealthCare has previously communicated End of Guaranteed Service for these Impacted Systems.
|
FDA
Z-1044-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Dec 10, 2025
|
Details |
|
SMV BodyTrack, System, Tomography, Computed, Emission
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affected Product Details section of this letter) could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury. There have been no reports of detector falls or injuries as a result of this potential issue. The Impacted Systems affected by this notice are those that have not been manufactured for several years. GE HealthCare has previously communicated End of Guaranteed Service for these Impacted Systems.
|
FDA
Z-1046-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Dec 10, 2025
|
Details |
|
Medline medical procedure convenience kits labeled as: 1) WCH BARI-GASTRECTOMY CDS, REF CDS860237AF; 2) ROBOTIC PROCEDURE, REF CDS982128Q; 3) CUH THORACIC, REF CDS984338M; 4) THORACIC PROCEDURE, REF CDS984640I; 5) DAVINCI ROBOTIC PACK-LF, REF DYNJ0525321O; 6) LAP CHOLE PACK, REF DYNJ57640F; 7) GYN/PROSTATE ROBOTIC PACK, REF DYNJ62594D; 8) RR-DAVINCI PROSTATE ACCESSORY, REF DYNJ63392D; 9) LAPAROSCOPY PACK, REF DYNJ68187B; 10) LAPAROSCOPY PACK, REF DYNJ82368A; 11) ROBOTIC KIDNEY PACK, REF DYNJ85261; 12) DOWNTOWN ROBOTICS, REF DYNJ86178B; 13) DAVINCI LITHOTOMY PACK, REF DYNJ87610; 14) ROBOTIC WHI
Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) during use.
|
FDA
Z-1087-2026
|
Medical Device | High |
Jan 21, 2026
Recall: Dec 16, 2025
|
Details |
Use brand, product name, UPC, lot code, best-by date, package size, allergen, contamination issue or distribution state.
Cars & equipmentSearch campaigns by make, model, year, component or NHTSA number. Use NHTSA's VIN search for vehicle-specific open recall status.
Family safetyCheck cribs, loungers, strollers, toys, formula, baby food and child car seats by brand, model, date code or hazard.
Fresh updatesBrowse new and recently updated notices across consumer products, foods, vehicles, medical devices and household items.
Start broad with the product name, manufacturer, retailer brand or model family. This is usually the fastest way to find a possible notice.
For food, drugs, cosmetics and packaged goods, compare the UPC, lot code, product code, best-by date, use-by date and package size.
For appliances, electronics, toys, furniture and baby products, match the model number, serial range, date code, color, size and retailer listing.
This site can find vehicle recall campaigns. For your exact car, use the official NHTSA VIN lookup to confirm unrepaired recall status.
Consumer products, toys, furniture, appliances, electronics and baby products. CPSC remedy details can change after a notice is first posted.
FDA-regulated foods, drugs, cosmetics and medical devices. FDA notes that not every recall has a press release on the public recalls page.
Meat, poultry and egg product recalls and public health alerts. Check establishment numbers, lot codes, labels and affected states.
Vehicle, tire, equipment and child-seat campaigns. VIN or license plate lookup is needed to know whether your specific vehicle still needs repair.
Use the brand, product name, manufacturer or retailer. If the result list is long, add a code from the label or package.
Read the product description, recall reason, hazard, affected dates, source agency and official recall number before taking action.
Compare the UPC, lot, best-by date, establishment number, model, serial range, color, size, state, retailer and product photo.
The notice may say stop using, do not eat, discard, return for refund, request a repair kit, replace a part or schedule dealer service.
Do not rely on brand alone. Match the package size, UPC, lot code, best-by date, use-by date, distribution states and any allergy or contamination warning.
Look for model number, date code, serial range, color, size, online listing, product photo and the exact hazard such as choking, suffocation, fire or fall risk.
Use campaign results to understand the issue, then verify your VIN, car seat model or tire information with NHTSA or the manufacturer.
Your item may not be part of that specific recall. Check spelling, older notices, retailer alerts and the official source before deciding it is safe.
A product recall is a safety or compliance notice saying a product may need to be corrected, removed, returned, repaired, replaced, refunded or discarded.
If all affected details match, follow the official instructions. Keep packaging, take photos, save receipts and contact the company or retailer when a refund or repair is offered.
A similar brand or product name is not enough. UPCs, lot codes, dates, model numbers, serial ranges and distribution areas determine whether your item is included.
Be careful with text messages, social posts or refund forms that ask for private information. Verify the notice through an official agency, retailer or manufacturer page.
Yes, when the official recall notice includes a UPC or product code. If no result appears, also search the brand, product name, package size, lot code and company name.
Yes. Lot codes are especially useful for food, drug, cosmetic and pet food recalls because only certain production batches may be affected.
No. This tool helps find vehicle recall campaigns and NHTSA numbers. Use the official NHTSA VIN or license plate lookup for vehicle-specific unrepaired recall status.
The database combines multiple official U.S. sources, but agencies and companies can publish or update notices at different times. Always check the linked official notice before taking final action.