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

Latest Product Recall Matches

Showing 376 - 400 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
ENDOVASCULAR PACK; Model/Item Number (Kit): VAPX014-04; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0095-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
BeneVision Series Telemetry Monitor. Operator's Manuals: TM70/TM80 Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions	FDA Z-0111-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 31, 2026	Details
DAVINCI LAP/GYN; Model/Item Number (Kit): WRNM037-16; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0101-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000; During use of an affected tube, the operator may encounter increased resistance when inserting the pipette. The resulting pressure buildup may cause the tube cap to detach or be forcibly ejected, potentially resulting in the release of blood and exposure of the operator or surrounding work area to a biological hazard (blood).	FDA Z-0107-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 25, 2026	Details
DxC 500i Clinical Analyzer Modules: 1. DxC 500 AU Module w/ISE, DxC 500i, Part No. C63522 2. DxC 500 AU Module, DxC 500i, Part No. C63521 3. Access 2 Module, DxC 500i, Part No. C13252 Beckman Coulter has identified a software issue affecting DxC 500i Clinical Analyzers when testing plasma samples. Following user configuration of a Clinical Chemistry test to use units different from the system default, a subsequent configuration change and activation of the draft configuration in the System Configuration page may cause the analyzer to revert the test units to the system default setting without notifying the user. The system does Pre-Review Reminders Include OII and [email protected] in any discussions on change/elevation of recalls to Class I classification and situations involving additional public communications (FDA and/or firm issued). Post-Review Reminders Final Check: Ensure your documentation accurately reflects the final recommendation prior to signature. Complete CTS: Recall Product tab, Additional Recall Event Info, Regulation, and Act. Upload PDFs of Consult, Review Memo, and Classification Letter for Class I Recall in DocMan. [Click to enter extra reminder]To add reminders, type the reminder in the text field to the left then press the Tab key. Doc ID 03534.05.06 2 of 8 not provide a warning or notification to alert the user that the configured units have reverted to the default units. This issue can result in falsely elevated reported results.	FDA Z-0083-2027	Medical Device	High	Oct 14, 2026 Recall: Sep 2, 2026	Details
Presource Packs containing Medtronic Microstream Components: Intubation Kit Catalog Numbers AN23366084 AN23366085 AN2336608H AN2336608J Intubating Bag Kit Catalog Number OMSVM4166A Intubation UH Kit Catalog Number AN2336608G Kits contain Microstream components. Medtronic issued an update to the Instructions for Use of these components due reports of difficulty in disconnecting the adapter from the patient's endotracheal tube to perform a procedure. The issue can result in a delay to treatment and unintended extubation. The potential exists for respiratory failure, hypoxia, aspiration, or low oxygen saturation.	FDA Z-0079-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 19, 2026	Details
Panorama and Telemetry Monitoring System. Operator's Manuals: TMS-6016/Panorama Telepack-608/TMS60 (TD60). Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions	FDA Z-0112-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 31, 2026	Details
MAJOR PACK; Model/Item Number (Kit): NIHB0018-11; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0104-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
Generic Name: Kit, Urine, Clean Catch Trade Name: Kit: Urinary Clean Catch 20/cs Model/Catalog Number: 76769 Lot Number: 333606 UDI-DI: 20809160118228 Software Version: N/A An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027.	FDA Z-0069-2027	Medical Device	High	Oct 14, 2026 Recall: Jul 9, 2026	Details
GYN LAPAROSCOPY/LAPAROTOMY; Model/Item Number (Kit): 1. WRNM002-15, 2. FBCH108-03; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0093-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
BeneVision N1 and N-Series Patient Monitor. Patient Monitor: N12/N15/N17/N19/N22. Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions	FDA Z-0110-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 31, 2026	Details
ABD HYSTERECTOMY; Model/Item Number (Kit): NAMC438-07; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0106-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
GYN LAPAROSCOPY PACK; Model/Item Number (Kit): NAMC436-12; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0105-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
Rollator, Bariatric, Basic Steel, Burgundy, mechanical walker with four legs and a metal frame intended for medical purposes to provide moderate weight support while walking, Product Number MDS86800XWS The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from the rollator frame tubing, the front wheels may become loose or detach from the rollator. If the front wheels become loose or detach during use, there is risk of severe adverse events. The immediate consequences could include falls resulting in head trauma, bone fractures, or other critical injuries.	FDA Z-0086-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 14, 2026	Details
VERIFY Biological Steam Test Pack Model/Catalog Number: S3069 Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential hazard is that the biological indicator will show no growth, indicating that the steam cycle was effective, even if the steam cycle did not achieve the intended spore reduction	FDA Z-0075-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 31, 2026	Details
DAVINCI TRUCUSTOM BUNDLE; Model/Item Number (Kit): 1. SAMM064-27, 2. SAMM064-28; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0092-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
ePM Series Patient Monitor. Patient Monitor Series: ePM 10M/ePM 12M/ePM 12MA/ ePM 15M/ePM 10A Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions	FDA Z-0109-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 31, 2026	Details
UROLOGY MAJOR; Model/Item Number (Kit): WRNM058-10; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0103-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
HexaVue Focus Integration System, a single, all-in-one system that handles operating room video routing, surgical video integration, and environmental control, Software Version: 2.0.18 A software issue may result in unintended mismatch of patient information on manually printed images. Incorrect patient information appearing on printed images could create a documentation discrepancy or incorrect association of clinical images with a patient record.	FDA Z-0118-2027	Medical Device	High	Oct 14, 2026 Recall: Sep 23, 2026	Details
CRANIOTOMY PACK; Model/Item Number (Kit): WRNM035-20; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0096-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers.	FDA Z-0090-2027	Medical Device	High	Oct 14, 2026 Recall: Jul 24, 2026	Details
ADULT HEART TRAY SHANDS JACKS; Model/Item Number (Kit): SHND419-08; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0094-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007 Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential hazard is that the biological indicator will show no growth, indicating that the steam cycle was effective, even if the steam cycle did not achieve the intended spore reduction	FDA Z-0071-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 31, 2026	Details
ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11; Product may be potentially contaminated with a lubricant used during the manufacturing process.	FDA Z-0098-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 10, 2026	Details
VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060 Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential hazard is that the biological indicator will show no growth, indicating that the steam cycle was effective, even if the steam cycle did not achieve the intended spore reduction	FDA Z-0072-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 31, 2026	Details

Showing 376 - 400 of 4,622 product recalls

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Fresh updates

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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

Consumer products, toys, furniture, appliances, electronics and baby products. CPSC remedy details can change after a notice is first posted.

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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