HIGH
FDA DEVICE
CUSA Clarity C7000 Console, Software Version: 2.1.1.909. Ultrasonic surgical aspirator system.
Software issue that renders the touch screen unresponsive.
Integra LifeSciences Corp.
Software issue
Recall database
All Product Recalls
Browse 4,434 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
- Active recalls
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- 74
HIGH
FDA DEVICE
The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.
In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.
Uvlizer c/o RAIS INTERNATIONAL
In some
Food & Beverages
HIGH
FDA FOOD
Distribuidora de Alimentos Sendero Recalls 500 Doraditas de Azucar for Allergen Labeling (2026)
Distribuidora de Alimentos Sendero LLC recalled 500 Doraditas de Azucar sold in Texas. The products are missing Wheat and Soy allergen labeling on the package. Consumers should not eat them and should contact Sendero LLC for refund or replacement.
Distribuidora de Alimentos Sendero
Gorditas and
Food & Beverages
HIGH
FDA FOOD
Distribuidora de Alimentos Sendero Recalls 2,500 Gorditas de Azucar UPC 860010238134 (2026)
Distribuidora de Alimentos Sendero LLC recalls 2,500 Gorditas de Azucar and Doraditas distributed in Texas. The recall is due to missing Wheat and Soy allergens on the label. Consumers should stop using it and contact Sendero LLC for refund or replacement.
Distribuidora de Alimentos Sendero
Gorditas and
HIGH
FDA DEVICE
The product is a handheld ultraviolet-C germicidal wand and contains a combination of five UV-A and UV-C LED lights. The product comes in two configurations: UV-C x 1; UV-A x 4, or UV-C x 2; UV-A x...
In some foreseeable use conditions, the products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.
Uvlizer c/o RAIS INTERNATIONAL
In some
HIGH
FDA DRUG
Semaglutide-Glycine-Cyanocobalamin Injectable, 2.5 mg, 5 mg, 1 MG/ML, 0.5 mL vials, Rx only, Northwest Compounders, Beaverton, OR
Lack of Assurance of Sterility
PAYLESS COMPOUNDERS
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Recall: Cook Staged Extubation Set Labeled with Expired Dates in 2026 Class II Recall
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray Recalled Over Expired-Lot
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Wayne Pneumothorax Set Recalled for Expired Shelf Life Labels
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Spectrum Central Venous Catheter Tray Recalled for Expired Shelf Life Labels (2026)
Cook Medical recalled 1,872 units of Spectrum Central Venous Catheter Trays worldwide due to expiration dates labeling that exceed true shelf life. Healthcare providers should stop using affected lots immediately and follow manufacturer instructions."
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Wayne Pneumothorax Tray Recalled for Expired-Labeled Shelf Life (2026)
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Recall: Strange Bile Duct Stone Exploration Set Labeled with Expired Dates (Z-1784-2026
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Approach CTO-12 Micro Wire Guide Recall Affects 49 Units for Expired Shelf-Life Labels
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical NCompass Nitinol Stone Extractor Recalled Over Expiration Date Shelf-Life Concerns (202
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Set Recall Affects 484 Units (Z
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Multipurpose Drainage Catheter Recalled Over Expired Labeling in Lots G29775
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Blue Rhino G2-Multi Tracheostomy Introducer Set Recalled for Expiration Date Labeling —
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Tornier Tornier HRS Max Parts Recalled for Mislabeling, Incompatibility (2026)
Affected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are incompatible with the Tornier HRS Max system.
Tornier
Affected products
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical CTO-18 Micro Wire Guide Recall Affects 75 Units Over Expired Dating (2026)
Cook Medical recalled 75 CTO-18 Micro Wire Guide devices distributed worldwide. The recall cites expiration date labeling that exceeds the true shelf life. Healthcare providers should stop using affected lots immediately and follow manufacturer instructions.
Cook
Products from
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Arterial Pressure Monitoring Tray Recalled Over Expired Shelf-Life Labeling (Z-1778-202
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from