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. 2,563 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,563 in last 12 months

Showing 1458114600 of 49,677 recalls

Medical DeviceSeptember 20, 2021· Arrow International Inc

Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...

The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2021· Arrow International Inc

Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...

The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2021· Arrow International Inc

Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...

The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Advia Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...

The Issue: The firm has confirmed the potential for ADVIA Chemistry...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by Siemens...

The Issue: The firm has confirmed the potential for Atellica CH Urinary/Cerebrospinal...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2021· Smith & Nephew, Inc.

Recalled Item: 6.5MMX165MM CANNULATED SCREW Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The product label incorrectly indicated that the screws are fully threaded,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 17, 2021· American Health Packaging

Recalled Item: GlipiZIDE Extended-Release Tablets Recalled by American Health Packaging Due...

The Issue: Failed Dissolution Specifications: results were above specification.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2021· Fresenius Kabi USA LLC

Recalled Item: Morphine Sulfate Injection Recalled by Fresenius Kabi USA LLC Due to...

The Issue: Defective container: Cracked vials leading to lack of sterility assurance

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 17, 2021· Bio-Rad Laboratories, Inc.

Recalled Item: BIO-RAD BioPlex 2200 Syphilis Total & RPR Calibrator Recalled by Bio-Rad...

The Issue: Due to two issues: 1) Customer complaints associated with greater than...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2021· Bio-Rad Laboratories, Inc.

Recalled Item: BIO-RAD BioPlex 2200 SYPH T PACK Syphilis Total Recalled by Bio-Rad...

The Issue: Due to two issues: 1) Customer complaints associated with greater than...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2021· Elekta, Inc.

Recalled Item: Elekta Medical Linear Accelerator (EMLA) Recalled by Elekta, Inc. Due to...

The Issue: There is a risk that the Diode D1 in the Modulator can fail in a destructive...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodSeptember 16, 2021· The Earl of Sandwiches

Recalled Item: Earle of Sandwiches Mild Smoked Jalapeno Sub Recalled by The Earl of...

The Issue: Sandwiches may contain undeclared soy and egg.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 16, 2021· The Earl of Sandwiches

Recalled Item: Duke of Earle Spicy Chicken Sub Recalled by The Earl of Sandwiches Due to...

The Issue: Sandwiches may contain undeclared soy and egg.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 16, 2021· The Earl of Sandwiches

Recalled Item: Earle of Sandwiches X-Large Roast Beef Italiano Recalled by The Earl of...

The Issue: Sandwiches may contain undeclared egg.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 16, 2021· The Earl of Sandwiches

Recalled Item: Duke of Earle X-Large Ham & Cheese Recalled by The Earl of Sandwiches Due to...

The Issue: Sandwiches may contain undeclared soy and egg.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 16, 2021· The Earl of Sandwiches

Recalled Item: Earle of Sandwiches X-Large Oven Roasted Turkey Recalled by The Earl of...

The Issue: Sandwiches may contain undeclared soy and egg.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 15, 2021· American Health Packaging

Recalled Item: Valproic Acid Oral Solution Recalled by American Health Packaging Due to...

The Issue: CGMP Deviations: Potential concern with products manufactured using liquid...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 14, 2021· Bayer Medical Care, Inc.

Recalled Item: The MEDRAD Twist & Go Disposable Syringe 150 mL with Recalled by Bayer...

The Issue: Labeling error: MEDRAD Mark 7 Arterion Injection System Syringes (ART 700...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2021· Elekta Inc

Recalled Item: Elekta Monaco - Product Usage: used to make treatment plans Recalled by...

The Issue: Contour changes can be saved on an unintended image set. In addition, these...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 13, 2021· Viatris

Recalled Item: Candesartan Cilexetil Tablets Recalled by Viatris Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; out of specification for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund