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

Latest Product Recall Matches

Showing 576 - 600 of 3,318 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-6316 Product Description: Feeding Tube Kit Component: No Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2340-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Plum Duo Precision IV Pump, 40002-0403 Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.	FDA Z-2313-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 29, 2026	Details
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2342-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320 Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2333-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316 Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2336-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Model/Catalog Number: 1023770 Software Version: N/A Product Description: The SporeTraq Mail-In Spore Testing Service includes 12 bacterial Spore Strips provided by Mesa Labs. The Spore Strip (single species G. stearothermophilus ATCC#7953 or dual species G. stearothermophilus ATCC #7953 and B. atrophaeus ATCC #9372) is intended for use in testing the efficacy of sterilizer systems used in healthcare facilities. The Spore Strips are compatible with Steam sterilization, C Due to incorrect incubation process being performed on product.	FDA Z-2332-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 13, 2026	Details
Allia IGS 5 Pulse angiographic X-ray system GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.	FDA Z-2315-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 20, 2026	Details
Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoassay A potential positive bias in quality control (QC) and patient sample results in three lots of the Dimension Tacrolimus (TAC) Flex reagent cartridge.	FDA Z-2398-2026	Medical Device	High	Jun 17, 2026 Recall: May 7, 2026	Details
CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930 Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.	FDA Z-2327-2026	Medical Device	High	Jun 17, 2026 Recall: May 1, 2026	Details
Boston Scientific TCN Electrodes: REF: TCN-5, TCN Electrode, NITINOL, 5 cm x 0.45 mm (0.0175 in); REF:TCN-10, TCN Electrode, NITINOL, 10 cm x 0.45 mm (0.0175 in) REF:TCN-15, TCN Electrode, NITINOL, 15 cm x 0.45 mm (0.0175 in); REF:TCN-20, TCN Electrode, NITINOL, 20 cm x 0.45 mm (0.0175 in) REF: TCN-5-3m, TCN Electrode, NITINOL, 3M CABLE, 5 cm x 0.45 mm (0.0175 in) REF: TCN-10-3M, TCN Electrode, NITINOL, 3M CABLE, 10 cm x 0.45 mm (0.0175 in); REF: TCN-15-3M, TCN Electrode, NITINOL, 3M CABLE, 15 cm x 0.45 mm (0.0175 in) REF: TCN-20-3M, TCN Electrode, NITINOL, 3M CABLE, 20 cm x 0.45 mm (0.0175 in Reusable electrodes may not meet expected performance levels.	FDA Z-2403-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 29, 2026	Details
MOSAIQ Oncology Information System Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.	FDA Z-2406-2026	Medical Device	High	Jun 17, 2026 Recall: May 21, 2026	Details
Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Model/Catalog Number: 1023780 Software Version: N/A Product Description: The SporeTraq Mail-In Spore Testing Service includes 52 bacterial Spore Strips provided by Mesa Labs. The Spore Strip (single species G. stearothermophilus ATCC#7953 or dual species G. stearothermophilus ATCC #7953 and B. atrophaeus ATCC #9372) is intended for use in testing the efficacy of sterilizer systems used in healthcare facilities. The Spore Strips are compatible with Steam sterilization, C Due to incorrect incubation process being performed on product.	FDA Z-2331-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 13, 2026	Details
Allia Moveo angiographic X-ray system GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.	FDA Z-2318-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 20, 2026	Details
Halyard, Pain Pack. Kit Code: AMPK48-01. Inadvertent distribution of sealed pouches that had not undergone validated sterilization.	FDA Z-2407-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
TDC VELOCE", 27G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT27, 9311.27G01, 9311.27G02, 9311.27K01, 9311.27K02, 9311.27K03, 9627.G0101, 9627.G0201, 9311.27G01-00; An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.	FDA Z-2324-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Allia IGS Pulse angiographic X-ray system GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.	FDA Z-2317-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 20, 2026	Details
Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A Software Version: 1.0.20 Product Description: The EXENT Analyser is an automated analyser intended for the qualitative and quantitative in vitro measurement of analytes in human body fluids used in conjunction with the EXENT assays. It was reported that plates 2 and 3 were marked as passed , although it appeared that QC had not been performed on these plates, despite samples being measured. The potential clinical hazards include false or missed detection of M-protein (false positive); and falsely elevated or decreased M-protein concentration.	FDA Z-2362-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 16, 2026	Details
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PUSH OTW Model/Catalog Number: 8170-24 Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2349-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PUSH OTW Model/Catalog Number: 8170-14 Product Description: Feeding Tube Kit Component: No Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2347-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Halyard, Towel Six Pack. Kit Code: AMTS70-01. Inadvertent distribution of sealed pouches that had not undergone validated sterilization.	FDA Z-2408-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL Model/Catalog Number: 8180-24 Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2352-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100 A defect has been identified in the manufacture of the Fresh Roast Systems ColorTrack instrument model number BENCH R-100 which could under very rare specific misuse circumstances potentially allow human access to infrared laser light levels in excess of the safety Classification of the product.	FDA Z-2280-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 15, 2026	Details
TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03, 9623.G0201, 9623.G0202, 9623.K0201, 9311.23G01-00; An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.	FDA Z-2322-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312 Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2339-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312 Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2335-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details

Showing 576 - 600 of 3,318 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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