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

Latest Product Recall Matches

Showing 301 - 325 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
HemoslL AcuStar HIT-lgG(PF-4). Part Number: 0009800127. in vitro diagnostic Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples.	FDA Z-0001-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 3, 2026	Details
Generic Name: BioFire¿ Joint Infection (JI) Panel Generic Name: BioFire¿ Joint Infection (JI) Panel Model/Catalog Number: RFIT-ASY-0138 (30 Kit), RFIT-ASY-0135 (6 Kit) Software Version: N/A Product Description: Mulitple-type osteoarticular pathogen nucleic acid IVD, kit, nucleic acid technique (NAT) Component: N/A Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results	FDA Z-0150-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 12, 2026	Details
Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with an inert additive to yield a demineralized bone matrix (DBM) allograft product having a particular physical form and/or handling property. Grafton DBM Gel and Grafton Plus DBM Paste are produced from a powder form of DBM, while Grafton DBM Flex, Putty, Matrix, Crunch" and Orthoblend are produced from a fiber form of DBM Crunch" also contains demineralized bone chips/cubes, while Grafton DBM Orthoblend contains non-demineralized cancellous bone chips in addition to DBM. Grafton DBM and Grafton Plus DBM are Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to the presence of microbial organisms. While the batch passed finished product sterility testing Medtronic is retrieving any unused product manufactured from the donor tissue. Donor bone tissue tested positive for Clostridium butyricum and while tissue did undergo gamma radiation, if implanted, there is a possibility of clostridium infection	FDA Z-0137-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 12, 2026	Details
Medline surgical convenience kits labeled as: 1) MAIN/LAPAROSCOPY TRANSPLA PACK, Medline product number/SKU DYNJ0656274AC; 2) MAIN/LAPAROSCOPY TRANSPLA PACK, Medline product number/SKU DYNJ0656274AB; 3) CATH LAB ENDO AAA, Medline product number/SKU DYNJ35312I; 4) MAIN/LAPAROSCOPY TRANSPLA PACK, Medline product number/SKU DYNJ0656274AA. Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.	FDA Z-0174-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 2, 2026	Details
Medline surgical convenience kits labeled as: 1) OPEN HEART CDS, Medline product number/SKU CDS840094R; 2) OPEN HEART CDS, Medline product number/SKU CDS840171AG; 3) MHC AV FISTULA, Medline product number/SKU DYNJ903705K; 4) PERIPHERAL VASC MAJR-LF, Medline product number/SKU CDS840379O; 5) MINOR VASCULAR PACK-LF, Medline product number/SKU DYNJ0349727D; 6) SJHC VASCULAR PK-LF, Medline product number/SKU DYNJ19906L; 7) CABG PACK-LF, Medline product number/SKU DYNJ0824648K; 8) PERIPHERAL VASC MNR-LF, Medline product number/SKU DYNJ22721N; 9) HEART A PACK, Medline product number/SKU DYNJ0362405S Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.	FDA Z-0170-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 2, 2026	Details
Medline surgical convenience kits labeled as: 1) NEURO-SPINE BASIN PACK, Medline Product Number/SKU DYNJ80055A; 2) AV SHUNT PACK-LF, Medline Product Number/SKU DYNJ24528M. Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.	FDA Z-0177-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 2, 2026	Details
Convenience Kits containing CONMED AirSeal Access Ports CHN GYN ONCOLOGY DYNJ906731K DYNJ906731L DYNJ906731N DAVINCI PROSTATECTOMY DYNJG901002A DYNJG901002B DYNJG901002C DYNJG901002D GENERAL DAVINCI DYNJG901004B DYNJG901004D HERNANDEZ DAVINCI ACC BUNDLE M DYNJ911258A KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116D DYKMBNDL116F ROBOTIC GYN DYNJ907827F ROBOTIC PACK DYNJ50474G RR-DAVINCI PROSTATE ACCESSORY DYNJ63392C DYNJ63392F Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.	FDA Z-0183-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 31, 2026	Details
DxU 840m Iris, REF: C76947; DxU 850m Iris, REF: C49513 The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however, the check valve replacement was excluded from the annual preventive maintenance (PM) requirements without adequate reliability evaluation. When the check valve is not replaced annually, it may allow lamina fluid to migrate internally and leak onto the table or floor, potentially resulting in exposure to physical hazards (slip/fall), chemical hazards (lamina fluid exposure), biohazardous exposure, property damage, and delayed patient results.	FDA Z-0160-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 12, 2026	Details
Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product Description: LIKORALL 242 ES, NATURAL Product Code: 3122005NA Product Description: LIKORALL 242 ES, NATURAL Product Code: 3122006 Product Description: LIKORALL 242 ES, WHITE Product Code: 3122006NA Product Description: LIKORALL 242 ES, WHITE Product Code: 3122007 Product Description: LIKORALL 242 ES R2R, NATURAL Product Code: 3122007NA Product Description: LIKORALL 242 ES R2R, NATURAL Product Code: 3122008 Product Description: LIKORALL 242 ES R2R, WHITE Product Code: 3122008NA Product Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift strap lowers more quickly than expected during use. Patients are at some risk for injury if a significant fall/drop were to occur due to this issue.	FDA Z-0151-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 14, 2026	Details
LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762. In kit sub-lot 2530M-01 the date of expiration printed on the outer labeling may indicate the wrong expiration date of July 22, 2026 while the correct expiration date is July 13, 2026. If used the system will display an error message and prevent the operator from running the test. Resulting in delayed results.	FDA Z-0162-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 4, 2026	Details
Medline surgical convenience kits labeled as: VEIN HARVESTING PACK, Medline product number/SKU DYNJ51845D Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.	FDA Z-0172-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 2, 2026	Details
Medline surgical convenience kits labeled as: OPEN HEART, Medline Product Number/SKU DYNJ902898D Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.	FDA Z-0178-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 2, 2026	Details
Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A CHN GYN ONCOLOGY DYNJ906731M Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.	FDA Z-0184-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 31, 2026	Details
Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A Discrepancy in the shelf-life of a component	FDA Z-0189-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 11, 2026	Details
Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with an inert additive to yield a demineralized bone matrix (DBM) allograft product having a particular physical form and/or handling property. Grafton DBM Gel and Grafton Plus DBM Paste are produced from a powder form of DBM, while Grafton DBM Flex, Putty, Matrix, Crunch" and Orthoblend are produced from a fiber form of DBM Crunch" also contains demineralized bone chips/cubes, while Grafton DBM Orthoblend contains non-demineralized cancellous bone chips in addition to DBM. Grafton DBM and Grafton Plus DBM are Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to the presence of microbial organisms. While the batch passed finished product sterility testing Medtronic is retrieving any unused product manufactured from the donor tissue. Donor bone tissue tested positive for Clostridium butyricum and while tissue did undergo gamma radiation, if implanted, there is a possibility of clostridium infection.	FDA Z-0138-2027	Medical Device	High	Oct 21, 2026 Recall: Aug 12, 2026	Details
Williams Cystoscopic Injection Needles, used for cystoscopic injection into the urethra, bladder neck, and bladder wall, Reference Part Number 090001-S26, Order Number (GPN) G16112 The female Luer lock adapter component in the affected device lots may not have been correctly seated due to misalignment and inadequate torquing during manufacturing. Potential events that may occur as a result of this issue include increased procedural time and inadequate treatment.	FDA Z-0163-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 16, 2026	Details
HemoslL AcuStar HIT-lgG(PF-4). Part Number: 0009802028. in vitro diagnostic (OUS only) Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples.	FDA Z-0002-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 3, 2026	Details
Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A & B, Medline Product number/SKU DYNJ04584L; 2) OPEN HEART ACCESSORY PACK, Medline Product number/SKU DYNJT5715A; 3) CABG ACCESSORY PACK, Medline Product number/SKU DYNJ85751; 4) OPEN HEART PACK, Medline Product number/SKU DYNJ53741N; 5) OPEN HEART PACK 1&2, Medline Product number/SKU DYNJ80701A; 6) VEIN PACK, Medline Product number/SKU DYNJ67308C; 7) OPEN HEART PACK, Medline Product number/SKU DYNJ89451B; 8) VASCULAR TRAY-LF, Medline Product number/SKU DYNJ42166A; 9) ENDOSCOPIC VEIN HARVEST PK, Medline Product number/SK Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.	FDA Z-0176-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 2, 2026	Details
Triathlon Hinge Femoral Prep Tray. Catalog Number: 6543-6-514. Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual moisture remaining after sterilization.	FDA Z-0166-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 16, 2026	Details
Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816 and PowerX2 Premium, Item No. 0015821 Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system not operating in powered mode, or exhibiting reduced powered performance. Issue may result in interruption or delay in patient transport.	FDA Z-0145-2027	Medical Device	High	Oct 21, 2026 Recall: Apr 28, 2026	Details
TS Universal Baseplate Finishing Tray, Triathlon. Catalog Number: 6543-6-506. Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual moisture remaining after sterilization.	FDA Z-0164-2027	Medical Device	High	Oct 21, 2026 Recall: Sep 16, 2026	Details
Unintended Vehicle Movement from Disengaged Electronic Parking Brake Koenigsegg Automotive AB (Koenigsegg) is recalling certain 2025-2026 CC850 vehicles. The electronic parking brake may not engage properly when the vehicle is in reverse, allowing in unintended vehicle movement. Unintended vehicle movement increases the risk of a crash or injury.	NHTSA 26V694000	Vehicle	High	Oct 21, 2026 Recall: Oct 21, 2026	Details
Fuel Filter Hoses May Disconnect and Leak Fuel Autocar, LLC (Autocar) is recalling certain 2022-2027 ACX (Xpeditor) vehicles equipped with Cummins L9 diesel engines, part number D563027BX03. The remote fuel filter hoses may separate from the fitting, causing a fuel leak and an engine stall. A fuel leak in the presence of an ignition source increases the risk of a fire. An engine stall increases the risk of a crash.	NHTSA 26V699000	Vehicle	High	Oct 21, 2026 Recall: Oct 21, 2026	Details
Wheel May Detach Hyundai Motor America (Hyundai) is recalling certain 2026 Venue, Elantra N, Elantra Hybrid, and Elantra vehicles. The wheel lug nuts may loosen and allow the wheel to detach. Wheel detachment can cause a loss of vehicle control or create a road hazard, increasing the risk of a crash or injury.	NHTSA 26V693000	Vehicle	High	Oct 21, 2026 Recall: Oct 21, 2026	Details
Loss of Drive Power from Unexpected Shift to Neutral Ford Motor Company (Ford) is recalling certain 2026-2027 Nautilus Hybrid and 2027 Corsair Hybrid vehicles. The vehicle may unexpectedly shift into neutral while driving, due to corrosion in the transmission's park lock actuator circuit board. A vehicle that unexpectedly shifts into neutral can lead to a sudden loss of drive power, increasing the risk of a crash.	NHTSA 26V688000	Vehicle	High	Oct 20, 2026 Recall: Oct 20, 2026	Details

Showing 301 - 325 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

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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

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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

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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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