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 21012120 of 49,677 recalls

Medical DeviceJune 30, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura R8.2.x Systems. Software Verion: R8.2.x. 1. Allura Xper FD10...

The Issue: Potential for temporary loss of imaging (X-ray) functionality due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2025· HeartSine Technologies Ltd

Recalled Item: HeartSine SAM 350P Recalled by HeartSine Technologies Ltd Due to Due to a...

The Issue: Due to a component manufacturing issue, Automated External Defibrillator may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2025· Philips North America

Recalled Item: Ingenia Ambition X Model Numbers (REF): (1) 781356 Recalled by Philips North...

The Issue: The potential for component failures in the Gradient Coil of the affected MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2025· Beyond Laser Systems, LLC

Recalled Item: Laser light show projectors manufactured by BLS Recalled by Beyond Laser...

The Issue: The remote interlock connector, which is required by 21 CFR 1040.10(f)(3),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2025· Beyond Laser Systems, LLC

Recalled Item: Laser light show projectors manufactured by BLS Recalled by Beyond Laser...

The Issue: The remote interlock connector, which is required by 21 CFR 1040.10(f)(3),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2025· Beyond Laser Systems, LLC

Recalled Item: Laser light show projectors manufactured by BLS Recalled by Beyond Laser...

The Issue: The remote interlock connector, which is required by 21 CFR 1040.10(f)(3),...

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

Class II — Potential Health HazardOngoing
DrugJune 27, 2025· Lupin Pharmaceuticals Inc.

Recalled Item: clomiPRAMINE Hydrochloride Capsules USP 25 mg Recalled by Lupin...

The Issue: Failed Impurities/Degradation Specifications: an out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2025· Sandoz Inc

Recalled Item: Cefazolin for Injection Recalled by Sandoz Inc Due to Labeling: Label...

The Issue: Labeling: Label Mix-Up; cartons of Cefazolin for Injection, USP 1 gram were...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2025· Sandoz Inc

Recalled Item: Buffered Penicillin G Potassium for Injection Recalled by Sandoz Inc Due to...

The Issue: Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 27, 2025· Maquet Cardiopulmonary Gmbh

Recalled Item: Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold...

The Issue: Device does not comply with the labeling requirements of international...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2025· Microbiologics Inc

Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to KWIK-STIK : 0894P, 0894K and...

The Issue: KWIK-STIK : 0894P, 0894K and LYFO DISK" 0894L may result in failure to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2025· Spiggle & Theis Mt Gmbh

Recalled Item: Injection needle Recalled by Spiggle & Theis Mt Gmbh Due to Affected product...

The Issue: Affected product show elevated cytotoxicity values. Use of affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2025· Microbiologics Inc

Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to KWIK-STIK : 0894P, 0894K and...

The Issue: KWIK-STIK : 0894P, 0894K and LYFO DISK" 0894L may result in failure to...

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

Class II — Potential Health HazardOngoing
DrugJune 26, 2025· AvKARE

Recalled Item: Pitavastatin Tablets Recalled by AvKARE Due to Failed Impurity/Degradation...

The Issue: Failed Impurity/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2025· AvKARE

Recalled Item: Pitavastatin Tablets Recalled by AvKARE Due to Failed Impurity/Degradation...

The Issue: Failed Impurity/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 26, 2025· Beckman Coulter Inc.

Recalled Item: UIBC (Unsaturated Iron Binding Capacity) Recalled by Beckman Coulter Inc....

The Issue: Beckman Coulter identified that the Unsaturated Iron Binding Capacity (UIBC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2025· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Wash/Waste Cartridge (4 Pack). Material Number:...

The Issue: Siemens Healthcare Diagnostics is recalling the RAPIDPoint 500 Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2025· Hamilton Medical AG

Recalled Item: Breathing circuit set Recalled by Hamilton Medical AG Due to Ventilator...

The Issue: Ventilator coaxial breathing circuit may have a crack in blue tubing, which...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 25, 2025· Preat Corp

Recalled Item: NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base Recalled...

The Issue: Engaging titanium base was manufactured 180 degrees around the post from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2025· Boston Scientific Corporation

Recalled Item: FARAWAVE 1.0 Pulsed Field Ablation Catheter Recalled by Boston Scientific...

The Issue: The potentially impacted units were manufactured using specific equipment...

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

Class II — Potential Health HazardOngoing