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

Latest Product Recall Matches

Showing 3,601 - 3,625 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Loss of Rearview Camera Image and ADAS Features Ford Motor Company (Ford) is recalling certain 2022-2025 Lincoln Navigator, 2024-2025 Lincoln Nautilus, 2025 Lincoln Aviator and Explorer vehicles. The Image Processing Module A (IPMA) may experience multiple unexpected resets, resulting in loss of the rearview camera image and advanced driver assistance (ADAS) features, including pre-collision assist, lane-keeping assist, and blind-spot monitoring. Loss of the rearview camera image and certain driver assistance features, can reduce the driver’s ability to detect hazards, increasing the risk of a crash.	NHTSA 26V165000	Vehicle	High	Mar 19, 2026 Recall: Mar 19, 2026	Details
Incorrect Seal Used on Axle During Assembly Lippert is recalling certain 8K axles. Please see the 573 Safety Recall Report for a full list of affected part numbers. The axle hubs were incorrectly assembled with a grease seal rather than an oil seal, causing oil to leak. A loss of lubrication can cause bearing failure and wheel loss, increasing the risk of a crash.	NHTSA 26E013000	Vehicle	High	Mar 19, 2026 Recall: Mar 19, 2026	Details
Body Panel Joint Incorrectly Attached/FMVSS 221 International Motors, LLC (International) is recalling certain 2023-2027 IC Bus CESB and 2025-2027 IC Bus EVSB school buses. The body panel joint may have been attached without sufficient epoxy coverage. As such these vehicle fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) No. 221, "School Bus Body Joint Strength." The body panels may separate during a crash, reducing structural integrity and increasing the risk of injury.	NHTSA 26V168000	Vehicle	High	Mar 19, 2026 Recall: Mar 19, 2026	Details
Specialized Bicycle Components Recalls Specialized Turbo Como SL Electric Bicycles Due to Risk of Serious Injury or Death from Fall Hazard This recall involves bicycle forks on all Specialized Como SL electric bicycles, regardless of model. "Como SL" is printed on the bicycle's seat tube or top tube, and the bikes were sold in a variety of colors, including Cast Umber, Dove Grey and Raspberry (Como SL 4.0), and Smoke, Brassy Yellow and Brushed Silver (Como SL 5.0). You can also determine which model you have by connecting your bicycle to the Specialized app. Only SL versions in the Como family of bicycles are part of this recall.	CPSC 10663	Consumer Product	High	Mar 19, 2026 Recall: Mar 19, 2026	Details
Lifetime Brands Recalls BUILT LUUM Light Up Tumblers Due to Risk of Choking and Battery Ingestion Hazards This recall involves the LUUM collection of BUILT-branded light up tumblers. The recalled plastic 16 oz. or 18 oz. drinking cups with a lid and a straw were sold in various winter holiday and Fourth of July themes. The tumblers have a bottom compartment containing a LED light that has a preinstalled button cell battery. "lumm," the tumbler's theme name and the following corresponding item numbers and UPC codes are printed on a label located on the tumblers' underside or hangtag: LUUM Tumbler Theme Capacity Item # UPC FESTIVE FOREST 18 oz 5323719 843461115513 MERRY GLOW 18 oz 5323721 843461115551 LET IT SNOW 18 oz 5323722 843461115520 WINTER BLOOM 18 oz 5323723 843461115537 MERRY MAGIC 18 oz 5323724 843461115544 JOLLY JOURNEY 18 oz 5323725 843461115568 HEART N STARS 18 oz 5331965 843461121002 USA 18 oz 5331966 843461121019 STARS 18 oz 5331967 843461121026 FLAG 18 oz 5331968 843461121033 WINDMILL 18 oz 5331969 843461121040 BLUE FIREWORKS 18 oz 5331974 843461121057 FESTIVE FOREST 16 oz 5324497 843461116374 MERRY GLOW 16 oz 5324498 843461116381 LET IT SNOW 16 oz 5324499 843461116398	CPSC 10664	Child/Baby	High	Mar 19, 2026 Recall: Mar 19, 2026	Details
Infant Walkers Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers; Sold on Amazon by Goregent Official Store This recall involves Goregent-branded infant walkers. The walkers are green and have a fabric seat with animal print, a rotating activity tray with toys, lights and music, a round base and six wheels. The walkers are collapsible with three adjustable height settings. "Model No: 901," "SKU: GEBA030AGXP" and "Date of Production: November 2025" are printed on a yellow label located on the walker's base.	CPSC 10665	Child/Baby	High	Mar 19, 2026 Recall: Mar 19, 2026	Details
Aisstxoer Adult Bicycle Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by YXTDZ Store This recall involves Aisstxoer bike helmets. The recalled helmets were sold in size large, fitting a head circumference of about 22.8 to 24.4 inches, and in the color pink. The recalled helmets have black padding, black straps, a black buckle and a black plastic knob at the back, for adjusting the fit. "Aisstxoer" and the size are printed on a white label on the packaging and the model "GH018L" is printed on a label located inside of the helmet.	CPSC 10668	Consumer Product	High	Mar 19, 2026 Recall: Mar 19, 2026	Details
Endo-Model Replacement Plateau; Item Number: 15-0027/16; The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.	FDA Z-1523-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 12, 2026	Details
Endo-Model Replacement Plateau; Item Number: 15-0027/12; The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.	FDA Z-1522-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 12, 2026	Details
Endo-Model Replacement Plateau; Item Number: 15-8521/11; The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.	FDA Z-1519-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 12, 2026	Details
GEM Premier 5000 PAK; Part No. 00055407504. Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.	FDA Z-1528-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 20, 2026	Details
EndoVive Safety PEG Kit; Outer Box Material Number (UPN): M00509001; Inner Box Material Number (UPN): M00509000; Recall of kits which utilized ChloraPrep Triple Swabsticks from BD. Open or compromised seals on the sterile swabstick packaging, which could result in loss of sterility or drying of the antiseptic solution. This component is placed outside of the sterile barrier of the tray manufactured by Boston Scientific, which contains the majority of the kit components. As such, inclusion of the affected ChloraPrep Triple Swabsticks does not degrade the integrity of the other components within the PEG kit.	FDA Z-1551-2026	Medical Device	High	Mar 18, 2026 Recall: Feb 10, 2026	Details
Wondfo Streptococcal A At-Home Self-Test. At-home test for group A beta-hemolytic streptococcal infection. Product not cleared by the FDA.	FDA Z-1559-2026	Medical Device	High	Mar 18, 2026 Recall: Dec 19, 2025	Details
Endo-Model Replacement Plateau; Item Number: 15-8521/09; The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.	FDA Z-1518-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 12, 2026	Details
Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2 The device does not bear a unique device identifier.	FDA Z-1505-2026	Medical Device	High	Mar 18, 2026 Recall: Aug 13, 2025	Details
Brand Name: Bisaf Strep A Self-Test. Test for detection of group A streptococcal antigens in throat swabs. Product not cleared by the FDA.	FDA Z-1561-2026	Medical Device	High	Mar 18, 2026 Recall: Dec 19, 2025	Details
Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5850.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot. Component: Not applicable. Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.	FDA Z-1550-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 9, 2026	Details
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02; The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.	FDA Z-1513-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 12, 2026	Details
GEM Premier 5000; Part No. 00055445010 & 00055445011. Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.	FDA Z-1543-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 20, 2026	Details
GEM Premier 5000 PAK; Part No. 00055415004. Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.	FDA Z-1532-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 20, 2026	Details
GEM Premier 5000 PAK; Part No. 00055360010. Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.	FDA Z-1526-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 20, 2026	Details
CLARITY II Laser System; Model No. 1110200210. Reports of devices sparking/popping and potentially burning patients.	FDA Z-1558-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 27, 2026	Details
Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTBTCS6090GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTDXUNDBGN DBD-DRAPE,UNDERBUTTOCK,28 X 50.5,XALT GR MDTMAYOXGN DBD-DRAPE,COVER,MAYO STAND,RESISTAT/XALT MDTZ1003656GN DBD-POCKET SHEET,RESISTAT/XALT Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may result in brief delay in patient care. If delaminated product is used and surgical strikethrough occurs, there may be risk of infection.	FDA Z-1564-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 28, 2026	Details
Endo-Model Replacement Plateau; Item Number: 15-2836/11; The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.	FDA Z-1516-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 12, 2026	Details
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/07; The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.	FDA Z-1514-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 12, 2026	Details

Showing 3,601 - 3,625 of 4,622 product recalls

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Browse new and recently updated notices across consumer products, foods, vehicles, medical devices and household items.

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

For food, drugs, cosmetics and packaged goods, compare the UPC, lot code, product code, best-by date, use-by date and package size.

Model, Serial Or Date Code

For appliances, electronics, toys, furniture and baby products, match the model number, serial range, date code, color, size and retailer listing.

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

Consumer Product Recalls

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FDA

Food And Medical Device Recalls

FDA-regulated foods, drugs, cosmetics and medical devices. FDA notes that not every recall has a press release on the public recalls page.

USDA FSIS

Meat, Poultry And Egg Product Recalls

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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