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. 2,666 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,666 in last 12 months

Showing 25612580 of 49,677 recalls

Medical DeviceApril 21, 2025· Capnia Inc

Recalled Item: Precision Sampling Set Recalled by Capnia Inc Due to Sampling set nasal...

The Issue: Sampling set nasal cannula used with End-Tidal Carbon Monoxide (ETCO)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2025· American Contract Systems, Inc.

Recalled Item: LOWER EXTREMITY Recalled by American Contract Systems, Inc. Due to Test...

The Issue: Test results for cast padding component included in procedure trays shows...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN...

The Issue: Due to a manufacturing defect IV catheter may have a hole in the septum,...

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

Class II — Potential Health HazardOngoing
DrugApril 18, 2025· FDC Limited

Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...

The Issue: Defective Container: Unable to get the solution out of the bottle as the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2025· American Regent, Inc.

Recalled Item: niCARdipine Hydrochloride Injection Recalled by American Regent, Inc. Due to...

The Issue: Lack of sterility assurance: Product leakage around the vial neck, which...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2025· American Regent, Inc.

Recalled Item: niCARdipine Hydrochloride Injection Recalled by American Regent, Inc. Due to...

The Issue: Lack of sterility assurance: Product leakage around the vial neck, which...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2025· Preferred Pharmaceuticals, Inc.

Recalled Item: Clindamycin Hydrochloride Capsules Recalled by Preferred Pharmaceuticals,...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: Ropivacaine Hydrochloride Injection Recalled by Amneal Pharmaceuticals, LLC...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard¿ Single Intragastric Linton Balloon Tube Recalled by C.R. Bard Inc Due...

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· Cook Incorporated

Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2025· Cook Incorporated

Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) Recalled by C.R....

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) Recalled by C.R. Bard...

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard Minnesota Four Lumen Esophagogastric Tamponade Tube Recalled by C.R....

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard Blakemore Esophageal-Nasogastric Tube (Adult) Recalled by C.R. Bard Inc...

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· Straumann USA LLC

Recalled Item: WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments....

The Issue: Incorrect blister labelling.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2025· Luminex Corporation

Recalled Item: VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test Recalled by...

The Issue: It was determined that the consumable issue may result in No Call - INT CTL...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2025· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus Pro Patient Monitor Recalled by Remote Diagnostic Technologies Ltd....

The Issue: software issue that causes an error screen on a portable vital signs monitor...

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

Class II — Potential Health HazardOngoing
FoodApril 15, 2025· Optimal Carnivore, LLC

Recalled Item: Bone & Joint Restore. 180 capsules in a plastic bottle. Recalled by Optimal...

The Issue: Potential for contamination with salmonella.

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2025· OurPharma LLC

Recalled Item: HYDROmorphone Hydrochloride 50mg/50mL (1mg/mL) Recalled by OurPharma LLC Due...

The Issue: Superpotent Drug: Assay/potency result for hydromorphone HCl in the...

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

Class III — Low RiskOngoing
Refund