Product Recalls Today
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Track recent product recall alerts from official U.S. sources. Filter by recall date, source agency, risk level and product category to find newly published food, vehicle, baby product, medical device and consumer product recalls.
Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
AirClub Convertible Bassinets Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violates Mandatory Standard for Bedside Sleepers
This recall involves AirClub convertible bassinets which convert into a bedside sleeper. The bassinets come in light grey, beige, and purple colors with quilted padding. "Product Model QX-831" is on a label located on the bottom of the convertible bassinets underneath the mattress pad.
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CPSC
10672
|
Consumer Product | High |
Mar 27, 2026
Recall: Mar 26, 2026
|
Details |
4our Kiddies Tip Restraint Kits Recalled Due to Tip-Over Hazard; Risk of Serious Injury and Death
This recall involves defective plastic tip restraint kits (also referred to as furniture straps) manufactured by 4our Kiddies. The recalled tip restraint kits contain two white plastic brackets/mounts (one for connection to furniture and the other for connection to the wall), a white plastic cable zip tie, two different pairs of screws (one longer than the other) and two drywall anchors. The plastic in the brackets/mounts and the cable zip tie can break or degrade over time, which could lead to furniture tipping over if a consumer interacts with furniture that was secured by the recalled product. CPSC testing revealed that the recalled plastic tip restraints failed to meet the requirements of the industry standard for tip restraints. CPSC's Anchor It! website, www.anchorit.gov/, has educational materials available to the public, including important instructions for properly anchoring furniture to prevent tip-overs.
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CPSC
10670
|
Child/Baby | High |
Mar 27, 2026
Recall: Mar 26, 2026
|
Details |
|
Park Outside: High Voltage Battery Modules May Short Circuit
Nissan North America, Inc. (Nissan) is recalling certain 2026 LEAF vehicles. The high voltage battery may have internal damage that can cause a short circuit within the battery module. A short circuit in a high voltage battery module increases the risk of a fire.
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NHTSA
26V188000
|
Vehicle | High |
Mar 26, 2026
Recall: Mar 26, 2026
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Details |
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Improperly Sealed Side Curtain Air Bags/FMVSS 226
Chrysler (FCA US, LLC) is recalling certain 2022-2026 Pacifica and Voyager vehicles. The right and left side curtain air bags may have insufficient pressure retention from improperly sealed seams. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 226, "Ejection Mitigation." Air bags with insufficient pressure retention increase the risk of ejection and injury during a crash.
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NHTSA
26V189000
|
Vehicle | High |
Mar 26, 2026
Recall: Mar 26, 2026
|
Details |
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Improperly Sealed Side Curtain Air Bags/FMVSS 226
Chrysler (FCA US, LLC) is recalling certain Mopar side curtain air bags with part numbers 68224526AJ and 68224527AH. The right and left side curtain air bags may have insufficient pressure retention from improperly sealed seams. As such, this equipment fails to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 226, "Ejection Mitigation." Air bags with insufficient pressure retention increase the risk of ejection and injury during a crash.
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NHTSA
26E014000
|
Vehicle | High |
Mar 26, 2026
Recall: Mar 26, 2026
|
Details |
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GAWR on Federal Placard May Exceed Tire Load Rating/FMVSS 120
Gillig, LLC (Gillig) is recalling certain 2023-2024 Low Floor transit buses equipped with Michelin X InCity Grip D rear tires. The rear Gross Axle Weight Rating (GAWR) on the federal placard may exceed the tire load rating. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 120, "Wheels and Rims - Other Than Passenger Cars." Referencing an incorrect GAWR can lead to unintentionally overloading the rear tires, increasing the risk of a crash.
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NHTSA
26V190000
|
Vehicle | High |
Mar 26, 2026
Recall: Mar 26, 2026
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Details |
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Incorrect Glaze May Reduce Visibility Though Door/FMVSS 205
ABC BUS Inc is recalling certain 1999-2013 Van Hool C2045, 2004-2013 Van Hool T2145, 2013-2022 Van Hool TX45, 2013-2023 Van Hool CX45, and 2016-2022 Van Hool CX35 vehicles. The front entrance door may have the incorrect glaze on the lower curb view window. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 205, "Glazing Materials." The incorrect glaze may reduce the driver's visibility, increasing the risk of a crash.
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NHTSA
26V191000
|
Vehicle | High |
Mar 26, 2026
Recall: Mar 26, 2026
|
Details |
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Incorrect Weld May Cause Seat Bracket Failure/FMVSS 207/210
Lucid USA, Inc. (Lucid) is recalling certain 2025-2026 Gravity vehicles. The lap belt anchor brackets on the second row seats may have insufficient welds, which can cause bracket failure. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 207, “Seating Systems” and 210, “Seat Belt Assembly Anchorages.” Seat bracket failure can increase the risk of injury during a crash.
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NHTSA
26V192000
|
Vehicle | High |
Mar 26, 2026
Recall: Mar 26, 2026
|
Details |
|
Disconnected Half-Shaft May Cause Loss of Drive Power
Lucid USA, Inc. (Lucid) is recalling certain 2024-2026 Air vehicles equipped with Pure Rear-Wheel Drive. Improperly secured bolts may allow the half-shaft to disconnect from the drive unit. A disconnected half shaft can result in a loss of drive power, increasing the risk of a crash.
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NHTSA
26V193000
|
Vehicle | High |
Mar 26, 2026
Recall: Mar 26, 2026
|
Details |
|
Fuel Hose May Disconnect and Leak Fuel
Honda (American Honda Motor Co.) is recalling certain 2025 CB1000SP motorcycles. The fuel feed hose may disconnect from the fuel tank, causing a fuel leak. A fuel leak near the rear tire can increase the risk of a crash or injury. In addition, a fuel leak in the presence of an ignition source increases the risk of a fire.
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NHTSA
26V194000
|
Vehicle | High |
Mar 26, 2026
Recall: Mar 26, 2026
|
Details |
|
Convatec, EsteemBody Drainable Pouch REF:423657 10-35mm
Drainable large pouch may leak due to manufacturing issue.
|
FDA
Z-1584-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Feb 16, 2026
|
Details |
|
Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 5826659-027, 5826659-029, 5826659-032, 5826659-033, 5826659-028, 5826659-034, 5826659-030, 5826659-019, 5826659-022, 5826659-026, 5826659-023, 5826659-031, 5826659-025, 5826659-002, 5826659-021, 5826659-037, 5826659-014, 5826659-016, 5826659-013
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
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FDA
Z-1569-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Jan 30, 2026
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Details |
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Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version: Software version 3.2.0.1 Product Description: Welch Allyn Spot Vision Screener VS100, FDA product code name: Refractometer, ophthalmic One unit per package
Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible individuals.
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FDA
Z-1573-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Feb 18, 2026
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Details |
|
Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version: Not Applicable Product Description: Influenza A/B virus nucleic acid IVD, kit, nucleic acid technique Component: Not Applicable
It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.
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FDA
Z-1565-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Feb 9, 2026
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Details |
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Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-026, 2088026-115, 2088026-043, K2042VJED, 2088026-132, 2088026-003, 2088026-110, 2089629-003, 2066908-136, 2066908-150
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
|
FDA
Z-1571-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Jan 30, 2026
|
Details |
|
Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585 Product Description: Aptima HPV assay Component: No
Due to product exhibiting potential to generate either invalid or false negative results.
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FDA
Z-1586-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Feb 18, 2026
|
Details |
|
Cub Pediatric Crib, Model FL19H
Cribs sold in the USA are missing two access door warning labels.
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FDA
Z-1580-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Feb 18, 2026
|
Details |
|
Artegraft Vascular Graft; REF#: AG740;
Labeling mix-up resulting in the incorrect lot outer packaging of product.
|
FDA
Z-1574-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Feb 10, 2026
|
Details |
|
Convatec, EsteemBody Drainable Pouch REF:423653 10-35mm
Drainable large pouch may leak due to manufacturing issue.
|
FDA
Z-1583-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Feb 16, 2026
|
Details |
|
Convatec, EsteemBody Drainable Pouch REF:423643, 10-45mm
Drainable large pouch may leak due to manufacturing issue.
|
FDA
Z-1582-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Feb 16, 2026
|
Details |
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Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF 00515 Product Description: The STA¿ - Liatest ¿ D-Di kit is an immuno-turbidimetric assay for the quantitative determination of D-dimer in venous plasma (in 3.2 % sodium citrate) for use on STA-R¿, STA Compact¿ and STA Satellite¿ analyzers by professional laboratory personnel. The STA¿ - Liatest¿ D-Di is intended for use in conjunction with a clinical pretest probability (PTP) assessment model to exclude pulmonary embolism (PE) and deep venous thrombosis (DVT) in outpatients suspected of PE or DVT. Component:
After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range.
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FDA
Z-1585-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Feb 5, 2026
|
Details |
|
Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-406, 2100169-001, 2088026-985, 2088026-971, 2088026-614, 2088026-713, 2088026-994, 2100491-006, 2088026-723, 2088026-308, 2104867-044, 2100491-012, 2088026-962, 2088026-969, 2102676-001, 2088026-936, 2088026-960, K1220JWED, 2088026-806, 2088026-506, 2088026-026, 2088026-970, 2088026-943, 2088026-990, 2088026-940, 2088026-959, 2088026-967, 2088026-989, 2104867-045, 2088026-993, 2088026-306, 2102675-010,
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
|
FDA
Z-1570-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Jan 30, 2026
|
Details |
|
Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell Gamma Knife¿ Elekta Esprit Leksell Gamma Knife¿ (available models Elekta Esprit, Icon", and Perfexion") is a radiosurgery system for use in the stereotactic irradiation of head structures. Surgery is achieved by delivering a prescribed dose as one or more shots of ionizing radiation to the exact site of the target.
Due to adapter not being properly aligned or locked in place.
|
FDA
Z-1581-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Feb 18, 2026
|
Details |
|
MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and detach from the attachment.
|
FDA
Z-1572-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Feb 2, 2026
|
Details |
|
Battery Charging Station; Model: 0998-00-0802;
The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to operate the IABP. Getinge has identified that a protruding screw in the left battery bay limits full insertion of certain batteries and prevents proper charging. The right bay of the Battery Charging Station is not affected by this issue.
|
FDA
Z-1587-2026
|
Medical Device | High |
Mar 25, 2026
Recall: Feb 6, 2026
|
Details |
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Recent recalls can include new notices, updated classifications, expanded lots, changed risk levels and public health alerts. Sort by newest first for the live recall feed view.
High-risk notices often involve serious injury, contamination, undeclared allergens, vehicle crash hazards, fire risks or products that should not be used or consumed.
This latest recall page combines CPSC, FDA, USDA FSIS and NHTSA data so shoppers do not need to check each agency page separately.
New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.
Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.
FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.
New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.
Recent recall pages are date-driven. Use the published date and recall date to understand whether an alert is new, newly classified or recently updated.
Choose food, vehicle, medical device, baby product, electronics, household or consumer product when the latest list is too broad.
Sort by highest risk when checking for urgent problems such as contamination, serious injury hazards, undeclared allergens, fire risks or vehicle safety defects.
Use the detail page and official source link before taking action. Agency notices may include exact lot codes, model ranges, remedy steps and company contacts.
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Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.
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