Product Recall Checker | Search Product Recalls by UPC, Lot Code, Brand or Model

Latest Product Recall Matches

Showing 3,401 - 3,425 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
ELENKER Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Fuzhou Shiahaha Cultural Industry Development This recall involves three different sizes of ELENKER-branded bed rails. The collapsible, portable adult bed rails are silver and come with a strap. Model HFK-5115 (SKU K90002C1) bed rails measure about 37.8 inches wide and 16.3 inches high. Model HFK-5116 (SKU K90001C1) bed rails measure about 28.5 inches wide and 16.3 inches high. Model HFK-5124 (SKU K90003C1) bed rails measure about 48.6 inches wide and 16.3 inches high. The SKU number is printed on the product packaging.	CPSC 10685	Consumer Product	High	Apr 3, 2026 Recall: Apr 2, 2026	Details
Coluans Christmas Light-Up Rings Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Toys; Sold on Amazon by BUDI Official This recall involves Coluans Christmas Light-Up Rings Party Favors, model number SJP-50. The light-up rings come with 50 multi-colored party favors, including light-up Santas, Christmas trees gingerbread men and other Christmas themed shapes. Each ring includes three preinstalled button cell batteries. The preinstalled button cell batteries are visible through the inner clear casing. The light-up rings have "SJP-50" and "SDJRJJZ0813" printed on labels located at the bottom of the packaging box.	CPSC 10683	Child/Baby	High	Apr 3, 2026 Recall: Apr 2, 2026	Details
Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violates the Small Ball Ban; Sold on Amazon by Beestech This recall involves Beestech's spiral children's tower toys. The toy has five multicolored levels and a basketball hoop with a character's face at the top. The toys measure about 10 inches high by four inches wide and come with six plastic balls. "Beestech" and model number "Bee-210316-01" are printed on the product's packaging.	CPSC 10681	Child/Baby	High	Apr 3, 2026 Recall: Apr 2, 2026	Details
Underbelly May Detach During Transit Keystone RV Company (Keystone) is recalling certain 2026 Montana fifth wheel recreational trailers. The underbelly may be improperly secured, causing it to detach. A detached underbelly can become a road hazard for other vehicles, increasing the risk of a crash.	NHTSA 26V211000	Vehicle	High	Apr 2, 2026 Recall: Apr 2, 2026	Details
Rearview Camera May Display Distorted or Blank Image General Motors, LLC (GM) is recalling certain 2023-2025 Chevrolet Malibu vehicles. The rearview camera screen may display a distorted or blank image. A rearview image that does not display correctly reduces the driver's view behind the vehicle, increasing the risk of a crash.	NHTSA 26V212000	Vehicle	High	Apr 2, 2026 Recall: Apr 2, 2026	Details
Missing Warning for Rear Turn Signal Failure/FMVSS 108 General Motors, LLC (GM) is recalling certain 2026 Chevrolet Corvette ZR1X Coupe, Corvette ZR1X Convertible, Corvette Coupe E-Ray, Corvette Convertible E-Ray, Corvette Convertible, Corvette Coupe, 2025 Corvette E-Ray Coupe, Corvette E-Ray Convertible, Corvette Convertible, and Corvette Coupe vehicles. A software error may prevent detection of a rear turn signal light failure. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Associated Equipment." The driver may be unaware that the turn signal is not working, increasing the risk of a crash.	NHTSA 26V213000	Vehicle	High	Apr 2, 2026 Recall: Apr 2, 2026	Details
Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device. Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.	FDA Z-1614-2026	Medical Device	High	Apr 1, 2026 Recall: Mar 2, 2026	Details
Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2" X 2" MSC8622EP DRESSING,COLLAGEN,PURACOL PLUS, 2X2.2" Elevated endotoxin levels identified in affected lots. Issue may elicit strong inflammatory response if used, including local tissue irritation, delayed wound healing, or systemic effects such as fever and hypotension. In severe cases, septic shock may result.	FDA Z-1650-2026	Medical Device	High	Apr 1, 2026 Recall: Feb 10, 2026	Details
Pelvic Reconstruction System (PRS) with the below descriptions and corresponding article numbers. 1. Fixation Screw; Article Number: 70312. 2. Spike short; Article Number: 70314. Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).	FDA Z-1600-2026	Medical Device	High	Apr 1, 2026 Recall: Jan 23, 2026	Details
Philips L12-5 Ultrasound Transducer To provide clarification and labelling to define the useful life of ultrasound transducers in the field.	FDA Z-1620-2026	Medical Device	High	Apr 1, 2026 Recall: Sep 5, 2025	Details
Brand Name: Olympus HALO PKS Cutting Forceps, 5mm 33cm Product Name: HALO PKS Cutting Forceps Model/Catalog Number: HACF0533 Product Description: The HALO PKS Cutting Forceps are intended to be passed through a 5 mm laparoscopic cannula. Coagulation is achieved using electrosurgical energy under laparoscopic visualization. The device is intended to be used with the Gyrus ACMI G400 Workstation only. Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.	FDA Z-1641-2026	Medical Device	High	Apr 1, 2026 Recall: Feb 25, 2026	Details
MicroScan Neg MIC 56 REF C42464 UDI-DI code: 15099590731212 MicroScan panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of aerobic and facultatively anaerobic gram-negative bacilli. Due to the likely presence of contamination in well(s).	FDA Z-1609-2026	Medical Device	High	Apr 1, 2026 Recall: Jul 24, 2025	Details
Volar Radius Plate with Angular Stability with the following description: Radius Plate PROlock II. Article Numbers: 21031-3, 21031-5, 21032-11, 21032-3, 21032-5, 21033-3, 21033-5, 21034-3, 21034-5, 21035-3, 21036-3. Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).	FDA Z-1592-2026	Medical Device	High	Apr 1, 2026 Recall: Jan 23, 2026	Details
Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use Probes may rupture/burst during activation	FDA Z-1567-2026	Medical Device	High	Apr 1, 2026 Recall: Feb 12, 2026	Details
Philips C9-4 Ultrasound Transducer To provide clarification and labelling to define the useful life of ultrasound transducers in the field.	FDA Z-1619-2026	Medical Device	High	Apr 1, 2026 Recall: Sep 5, 2025	Details
Brand Name: BiDop 3 Product Name: BiDop 3 Pocket Doppler (ES-100V3) with BT2M20S8C fetal probe Model/Catalog Number: ES-100V3 (device); BT2M20S8C (2 MHz fetal probe). Software Version: N/A Product Description: Hand-held, battery-powered ultrasonic Doppler blood-flow detector with LCD numeric display, used with interchangeable probes to detect vascular blood-flow signals and display heart rate; affected units were packaged with a 2 MHz BT2M20S8C fetal probe and labeled for both vascular and fetal applications. Product labeling includes a fetal indication for use that is not cleared under its 510(k).	FDA Z-1631-2026	Medical Device	High	Apr 1, 2026 Recall: Mar 4, 2026	Details
Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920005PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the PKS electrical generator. Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.	FDA Z-1644-2026	Medical Device	High	Apr 1, 2026 Recall: Feb 25, 2026	Details
Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord, 5mm 33 cm Product Name: Everest Bipolar Cutting Forceps Model/Catalog Number: 3006 Product Description: The OLYMPUS Everest Bipolar Cutting Forceps are intended to be passed through a 5 mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the bipolar outputs of compatible generators. Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.	FDA Z-1639-2026	Medical Device	High	Apr 1, 2026 Recall: Feb 25, 2026	Details
Pilonplate with Angular Stability, with the below descriptions and corresponding article numbers. 1. Anterolateral Tibia Plate; Article Numbers: 21311-11, 21311-15, 21311-7, 21312-11, 21312-15, 21312-7. 2. Pilon Plate 4mm; Article Numbers: 21094-10, 21094-4, 21094-6, 21094-8. 3. Pilon Plate, Small; Article Numbers: 21093-4, 21093-6. Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).	FDA Z-1596-2026	Medical Device	High	Apr 1, 2026 Recall: Jan 23, 2026	Details
Philips X7-2 Ultrasound Transducer To provide clarification and labelling to define the useful life of ultrasound transducers in the field.	FDA Z-1628-2026	Medical Device	High	Apr 1, 2026 Recall: Sep 5, 2025	Details
Philips 3D6-2 Ultrasound Transducer To provide clarification and labelling to define the useful life of ultrasound transducers in the field.	FDA Z-1618-2026	Medical Device	High	Apr 1, 2026 Recall: Sep 5, 2025	Details
FR.O.H. Calcaneus Repair System with the following description: Anterolateral Calcaneus Plate. Article Number: 21064-60. Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).	FDA Z-1595-2026	Medical Device	High	Apr 1, 2026 Recall: Jan 23, 2026	Details
Custom Abutment AS Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 010.5438; A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 / Lot 7130439) was incorrectly identified as a Titanium Bar Ti Gr4 D (SAP #701922 / Lot 7130430). As a result, RC Titanium abutments were manufactured using the TAN Bar material on Mill-from-Bar Machine 396-06.	FDA Z-1633-2026	Medical Device	High	Apr 1, 2026 Recall: Mar 17, 2026	Details
Embrace Drill Tower, Standard/Lateral (25mm); Item Number: 645-081/63; The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps described in the surgical technique are correct.	FDA Z-1652-2026	Medical Device	High	Apr 1, 2026 Recall: Feb 11, 2026	Details
I.T.S. DUL (Distal Ulna Locking) System and UOL (Ulna Osteotomy Locking) System with the below descriptions and corresponding article numbers. 1. I.T.S. DUL (Distal Ulna Locking) System, Distal Ulna Plate; Article Numbers: 21232-3, 21232-4, 21232-6, 21233-3, 21233-4, 21233-6, 21234-4, 21235-4. 2. I.T.S. UOL (Ulna Osteotomy Locking) System, Ulna Osteotomy Plate; Article Numbers: 21231-6. 3. UOL (Ulna Osteotomy Locking) System, Cancellous Screw, Locking; Article Numbers: 37302-18, 37302-20. Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).	FDA Z-1604-2026	Medical Device	High	Apr 1, 2026 Recall: Jan 23, 2026	Details

Showing 3,401 - 3,425 of 4,622 product recalls

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What To Enter In The Search Box

A recall usually applies to specific products, batches, model ranges or dates. Use the details printed on the item, package, label, receipt or vehicle paperwork.

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.

UPC, Lot Code And Dates

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Model, Serial Or Date Code

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VIN Or NHTSA Campaign

This site can find vehicle recall campaigns. For your exact car, use the official NHTSA VIN lookup to confirm unrepaired recall status.

Official Sources This Checker Organizes

The goal is to make official notices easier to search. The final decision should still come from the linked agency or manufacturer notice.

CPSC

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FDA

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USDA FSIS

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Meat, poultry and egg product recalls and public health alerts. Check establishment numbers, lot codes, labels and affected states.

NHTSA

Vehicle, Tire And Car Seat Recalls

Vehicle, tire, equipment and child-seat campaigns. VIN or license plate lookup is needed to know whether your specific vehicle still needs repair.

How To Confirm A Recall Match

1. Search The Obvious Name First

Use the brand, product name, manufacturer or retailer. If the result list is long, add a code from the label or package.

2. Open The Closest Result

Read the product description, recall reason, hazard, affected dates, source agency and official recall number before taking action.

3. Match Every Identifier

Compare the UPC, lot, best-by date, establishment number, model, serial range, color, size, state, retailer and product photo.

4. Follow The Official Remedy

The notice may say stop using, do not eat, discard, return for refund, request a repair kit, replace a part or schedule dealer service.

When A Recall Result Looks Like Your Product

Use this checklist before you throw away a product, call the company, request a refund or schedule a repair.

If It Is Food, Formula Or Pet Food

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.

If It Is A Baby Or Household Product

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.

If It Is A Vehicle Or Car Seat

Use campaign results to understand the issue, then verify your VIN, car seat model or tire information with NHTSA or the manufacturer.

If The Details Do Not Match

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.

What Is A Product Recall?

A product recall is a safety or compliance notice saying a product may need to be corrected, removed, returned, repaired, replaced, refunded or discarded.

What Should You Do After Finding A Recall?

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.

Why Recall Details Must Match Exactly

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.

How To Avoid Fake Recall Notices

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.

Product Recall FAQ

Short answers for common product recall searches.

Can I search product recalls by UPC code?

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.

Can I search product recalls by lot code?

Yes. Lot codes are especially useful for food, drug, cosmetic and pet food recalls because only certain production batches may be affected.

Does this replace a VIN recall lookup?

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.

Are all recalls listed here?

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.

Product Recall Checker: Search Recalls by UPC, Lot Code, Brand or Model

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