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

Latest Product Recall Matches

Showing 426 - 450 of 4,975 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
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
Glypto Device, Glypto Cryo Machine; Lack of 510(k) clearance.	FDA Z-0080-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 24, 2026	Details
VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3061 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-0073-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 31, 2026	Details
VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB006 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-0070-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 31, 2026	Details
Battle Bandage, REF: 32-700; Patrol IFAK Bag, Black - Advanced, REF: 81-125-BL; Patrol IFAK Bag, Multicam - Advanced, REF: 81-125-MC; Patrol IFAK II, Olive Drab, Stocked (Option 1), 81-129-OD; IFAK Bag, Intermediate, Black - Stocked, 81-133-BL; IFAK Bag, Intermediate, Coyote Brown - Stocked, 81-133-CB; IFAK Bag, Intermediate, Multicam - Stocked, 81-133-MC; IFAK Bag, Advanced, Black - Stocked, 81-135-BL; IFAK Bag, Advanced, Multicam - Stocked, 81-135-MC; LEO Patrol Kit, 81-139; IFAK Refill, 81-301; IFAK Resupply, 81-303-01; IFAK Resupply - CS/30, 81-303-30; K9 Trauma Kit, 81-605; Medic Enhancem Compression bandage may be degraded, which may cause unwanted foreign material to be introduced inside the wound, which may lead to wound exploration and irrigation, formation of scar tissue, and infection.	FDA Z-0081-2027	Medical Device	High	Oct 14, 2026 Recall: Sep 2, 2026	Details
Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station, Model/Catalog Number: CN-6201 Software Version: software versions: 01-03, 01-04, 01-05, 01-06, 02-10, 02-11, and 02-40 Product Description: The device is intended for use by medical professionals to provide cardiac and vital signs monitoring for multiple patients within a medical facility. The CNS-6200 Series Central Nurse Station will display and record physiological data from up to forty telemetry receiver/transmitters and generates an alarm when a measured parameter falls outside a pre-set limit or when life threatening arrhy Due to a cybersecurity issue associate with a NULL Pointer Dereferences vulnerabiity. If exploited would potentially cause disruption of the centralized monitoring of multiple beds and the visualization of alarms.	FDA Z-0089-2027	Medical Device	High	Oct 14, 2026 Recall: Sep 8, 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-0091-2027	Medical Device	High	Oct 14, 2026 Recall: Jul 24, 2026	Details
Rollator, Bariatric, Basic Steel, Blue, mechanical walker with four legs and a metal frame intended for medical purposes to provide moderate weight support while walking, Product Number MDS86800XWBS 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-0087-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 14, 2026	Details
Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model Numbers: 1. 728333 (U.S. and Outside U.S.), 2. 728340 (Outside U.S.), 3. 728344 (Outside U.S.), 4. 728345 (Outside U.S.); Software issues may affect the safety and performance of Spectral CT system(s). The issues may result in image artifacts, wrong slice thickness, or unintended system motion.	FDA Z-0078-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 21, 2026	Details
Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog Numbers: MMT-8062; MMT-8072 Product Description: The MiniMed Flex pump is an alternate controller enabled (ACE) pump intended for the subcutaneous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin. It can reliably and securely communicate with compatible digitally connected devices, including an integrated continuous glucose monitor (iCGM), interoperable Medtronic continuous glucose monitor (CGM), and interoperable automated glycemic controller (iAGC Some MiniMed Flex insulin pumps were released with missing (i.e., devices with no result or abort test results are presumed to have failed) or failed verification test results in one or more of 9 functional tests. The unverified/failed pumps released to users potentially have one or more of the following issues: inoperable pump at setup, lack of protection for moisture exposure, slow battery charging, disconnection issues with other system components (i.e., continuous glucose monitoring sensor or MiniMed mobile app), reduced ability to detect occlusion events, compromised audio for pump alarms/alerts, and/or inaccurate insulin delivery.	FDA Z-0088-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 20, 2026	Details
VERIFY Biological Steam Test Pack Model/Catalog Number: S3065 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-0074-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 31, 2026	Details
BARD EP XT DECAPOLAR STEERABLE, DIAGNOSTIC EP CATHETER, 6F, LARGE 4.0, 10, 2-5-2MM, REF: 201007 Diagnostic electrophysiology (EP) catheter may have a breached sterile barrier on the straight seal side of the primary pouch, which if used could lead to particulate embolization, infection, thrombus or ganuloma formation from particulate matter.	FDA Z-0085-2027	Medical Device	High	Oct 14, 2026 Recall: Aug 18, 2026	Details
Missing Circuit Protection on Charge Line K.Z., Inc. (K.Z.) is recalling certain 2026-2027 SportTrek Fifth Wheel recreational trailers. The charge line may not have circuit protection. An unprotected charge line can cause the wire to overheat, increasing the risk of a fire.	NHTSA 26V672000	Vehicle	Unknown	Oct 13, 2026 Recall: Oct 13, 2026	Details
Head Restraint Cushion May Detach Volvo Car USA, LLC (Volvo Car) is recalling certain 2025-2026 EX30 and 2026 EX30CC vehicles. The head restraint cushion may detach during a crash. A detached head restraint cushion can increase the risk of injury during a crash.	NHTSA 26V671000	Vehicle	High	Oct 9, 2026 Recall: Oct 9, 2026	Details
Incorrect Tire Size and Pressure Information on Label/FMVSS 110 Grand Design RV, LLC (Grand Design) is recalling certain 2027 Transcend travel trailers. The tire information label may state the incorrect tire size and cold inflation pressure. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 110, "Tire Selection and Rims." Referencing incorrect information can result in installing the wrong size replacement tires or underinflating the tires, increasing the risk of a crash.	NHTSA 26V668000	Vehicle	High	Oct 9, 2026 Recall: Oct 9, 2026	Details
Seating Power Cord May Have Inadequate Circuit Protection Lippert is recalling certain power seating assemblies. The power cord fuse may not provide adequate circuit protection. In the event of a short circuit, inadequate protection increases the risk of a fire.	NHTSA 26E070000	Vehicle	Unknown	Oct 9, 2026 Recall: Oct 9, 2026	Details
Park Outside: Fire from Overheated Power Seat Motors Hyundai Motor America (Genesis) is recalling certain 2015-2016 Hyundai Genesis, and 2017-2020 Genesis G80 vehicles. The front power seat motors may overheat due to a stuck power seat control switch, which can result in a fire while parked or driving. A fire increases the risk of injury.	NHTSA 26V664000	Vehicle	High	Oct 9, 2026 Recall: Oct 9, 2026	Details
Safety Chains Are Underrated For GVWR Grand Design RV, LLC (Grand Design) is recalling certain 2026-2027 Imagine travel trailers. The installed safety chains are underrated for the Gross Vehicle Weight Rating (GVWR). Underrated chains can allow the trailer to detach from the tow vehicle, increasing the risk of a crash.	NHTSA 26V667000	Vehicle	High	Oct 9, 2026 Recall: Oct 9, 2026	Details

Showing 426 - 450 of 4,975 product recalls

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Food safety

Food Product Recall Search

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Vehicle Recall Lookup

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Family safety

Baby Product Recall Alerts

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Fresh updates

Latest Product Recalls Today

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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