Product Recalls in Utah
Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,433 recalls have been distributed to Utah in the last 12 months.
Showing 34661–34680 of 49,677 recalls
Recalled Item: SurgiCounter scanner Recalled by Stryker Instruments Div. of Stryker...
The Issue: The affected scanner does not correctly interact with the SC360 software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioVac Circuit Pack (Tandem Packs) Recalled by Angiodynamics Inc....
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Surgery Pack Recalled by Windstone Medical Packaging, Inc. Due to...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Recalled by Windstone Medical Packaging, Inc. Due to These...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-10 360 SOFT 10MM X 20CM SR Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-18 360 11MM X 30CM Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex MEDICAL AngioVac Circuit Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Latex Free Recalled by Windstone Medical Packaging, Inc. Due...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded Recalled by Becton...
The Issue: The device may have a defect in the catheter. In some instances this defect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD-Retic-Count Reticulocyte Reagent System Recalled by Becton, Dickinson and...
The Issue: The carton label for one lot of BD Retic-Count Reticulocyte Reagent System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Ultraflex Tracheobronchial Distal Release Stent System...
The Issue: Mislabeled: 10mm diameter x 30mm length Ultraflex Tracheobronchial stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Hospira Inc. Due to Presence...
The Issue: Presence of Particulate Matter: particulate matter identified as an insect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibrate Capsules (Micronized) 134 mg Recalled by Impax Laboratories,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibrate Capsules (Micronized) 200 mg Recalled by Impax Laboratories,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chicken of the Sea 5 Oz. Canned Chunk Light Tuna in Water Recalled by...
The Issue: Tri-Union Seafoods LLC is voluntarily recalling a limited amount of Chicken...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chicken of the Sea 5 Oz. Canned Chunk Light Tuna in Oil Recalled by...
The Issue: Tri-Union Seafoods LLC is voluntarily recalling a limited amount of Chicken...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Thai Fusion Outpost Recalled by Paradise Farm Organics Inc Due to Undeclared...
The Issue: Organic Thai Fusion Outpost 5.1 oz. packages, Organic Thai Fusion 3 lbs....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dimension Assays: Direct HDL Cholesterol (AHDL) Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona The Personalized Knee System Articular Surface Posterior Stabilized...
The Issue: The firm received a customer complaint establishing that the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic 0-arm Imaging mobile x-ray system. Model Numbers - B1-700-00027...
The Issue: It has been discovered that replacement x-ray generator and system motion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.