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

Latest Product Recall Matches

Showing 1,876 - 1,900 of 3,321 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Allura Xper FD10C; System Code: 722001; Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1659-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
MEDLINE ANTERIOR HIP PACK DYNJ64672B Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.	FDA Z-1711-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 16, 2026	Details
MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851) All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.	FDA Z-1744-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 13, 2026	Details
Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation catheter renal denervation Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.	FDA Z-1654-2026	Medical Device	High	Apr 8, 2026 Recall: Jan 29, 2026	Details
Vue Motion V12. Product Number: 1017979. Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.	FDA Z-1692-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 5, 2026	Details
Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only); Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1678-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028; Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1663-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
Burlington Medical, BAT (Breast, Axilla and Thyroid) Coverage. Potential for attenuation degradation over time, decreasing the lifespan.	FDA Z-1758-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 11, 2026	Details
Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Model/Catalog Number: 420207 Software Version: N/A Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement of microw Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments	FDA Z-1700-2026	Medical Device	High	Apr 8, 2026 Recall: Dec 9, 2025	Details
Burlington Medical, Kilt Potential for attenuation degradation over time, decreasing the lifespan.	FDA Z-1755-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 11, 2026	Details
Allura Xper FD20/20; System Code: 722038; Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1669-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
Allura Xper FD20/15; System Code: 722058; Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1671-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device. In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.	FDA Z-1646-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 2, 2026	Details
Burlington Medical, Caps. Potential for attenuation degradation over time, decreasing the lifespan.	FDA Z-1760-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 11, 2026	Details
Medline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915 Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.	FDA Z-1708-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 16, 2026	Details
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001 Surgical light assembly may not adequate support the weight of the ceiling cover.	FDA Z-1688-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 23, 2026	Details
ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033; Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1667-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
Burlington Medical, Thyroid Shield. Potential for attenuation degradation over time, decreasing the lifespan.	FDA Z-1753-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 11, 2026	Details
eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149 There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.	FDA Z-1731-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 2, 2026	Details
ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027; Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1662-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
MiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892) All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.	FDA Z-1742-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 13, 2026	Details
Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Double Fenestrated Grasper Instrument Model/Catalog Number: 420189 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and pl Due to increased complaints for broken/frayed grip cables for reusable instruments.	FDA Z-1697-2026	Medical Device	High	Apr 8, 2026 Recall: Dec 9, 2025	Details
Sterile Radiology Procedure Kits, Model Number DYNDH1491B There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.	FDA Z-1693-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 18, 2026	Details
Brand Name: Finesse BTK Multicath Product Name: Injectable Angioplasty Balloon Catheter Model/Catalog Number: FS252251502 Product Description: 5 French sheath, 0.014" guidewire compatible over-the-wire injectable angioplasty balloon catheter, balloon diameter 2.5mm, balloon length 225mm, catheter working length 150cm Component: NA Potential for the balloon in the device to not meet burst specifications.	FDA Z-1704-2026	Medical Device	High	Apr 8, 2026 Recall: Jul 21, 2025	Details
Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro Laser System TFL-SLS Model/Catalog Number: TFL-SLS containing TFL-CSLU Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate soft tissue with moderate hemostasis, little charring, and a thin zone of necrosis. Component: No Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to become inoperable. Additionally, smoke or a burning smell may occur. By design, the issue causing the smoke or burning smell would be contained within the internal laser console enclosure and would be self-extinguishing.	FDA Z-1695-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 27, 2026	Details

Showing 1,876 - 1,900 of 3,321 product recalls

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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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