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. 2,627 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,627 in last 12 months

Showing 80618080 of 49,677 recalls

Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: API3200MD Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: Citrine QTRAP Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing
DrugAugust 29, 2023· RB Health (US) LLC

Recalled Item: Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%) Recalled by...

The Issue: Labeling: Label Error on Declared Strength: The incorrect label on the back...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 29, 2023· CooperSurgical, Inc.

Recalled Item: Box as labeled: Regard Recalled by CooperSurgical, Inc. Due to Incorrect...

The Issue: Incorrect component descriptions within the "Contents" section on the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2023· Flower Orthopedics Corporation

Recalled Item: Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to...

The Issue: Device is breaking while in use, potential for patients to require a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2023· Becton Dickinson Infusion Therapy Systems Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems Inc. Due to There is...

The Issue: There is the potential that the safety shield may not properly engage on IV...

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

Class II — Potential Health HazardOngoing
DrugAugust 26, 2023· Dr. Berne's Whole Health Products

Recalled Item: Dr. Berne's Organic Castor Oil Eye Drops Recalled by Dr. Berne's Whole...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2023· Dr. Berne's Whole Health Products

Recalled Item: Dr. Berne's MSM MIST 15% Solution Recalled by Dr. Berne's Whole Health...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2023· Dr. Berne's Whole Health Products

Recalled Item: Dr. Berne's MSM DROPS 5% Solution Recalled by Dr. Berne's Whole Health...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2023· Dr. Berne's Whole Health Products

Recalled Item: Dr. Berne's MSM DROPS 15% Solution Recalled by Dr. Berne's Whole Health...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 26, 2023· Dr. Berne's Whole Health Products

Recalled Item: Dr. Berne's MSM DROPS 5% Solution Recalled by Dr. Berne's Whole Health...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 25, 2023· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Clear Recalled by CareFusion 213, LLC Due to Stability data...

The Issue: Stability data does not support expiry: Shelf-life of the impacted lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2023· Hua Da Trading, Inc. dba Wefun Inc.

Recalled Item: WEFUN Capsules 825 mg Recalled by Hua Da Trading, Inc. dba Wefun Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 25, 2023· Marlex Pharmaceuticals, Inc.

Recalled Item: Digoxin Tablets Recalled by Marlex Pharmaceuticals, Inc. Due to Labeling:...

The Issue: Labeling: Label Mix-Up- Bottles labeled as Digoxin Tablets, USP 0.125 mg...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2023· Marlex Pharmaceuticals, Inc.

Recalled Item: Digoxin Tablets Recalled by Marlex Pharmaceuticals, Inc. Due to Labeling:...

The Issue: Labeling: Label Mix-Up- Bottles labeled as Digoxin Tablets, USP 0.125 mg...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 25, 2023· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem P Recalled by TECHNO-PATH MANUFACTURING LTD. Due to Technopath...

The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2023· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem S Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...

The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2023· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem IA Plus Recalled by TECHNO-PATH MANUFACTURING LTD. Due to...

The Issue: Technopath Manufacturing Ltd. has identified an issue with the glass vial...

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

Class II — Potential Health HazardOngoing
DrugAugust 24, 2023· Baxter Healthcare Corporation

Recalled Item: Doxil (doxorubicin hydrochloride liposome injection) 50 mg in 25 mL (2...

The Issue: CGMP Deviations: Product was exposed to temperatures exceeding the labeled...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 24, 2023· MICROVENTION INC.

Recalled Item: AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM Recalled by...

The Issue: Peripheral coil system detachable has a potential of unsealed pouch packaging.

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

Class II — Potential Health HazardOngoing