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 26212640 of 13,417 recalls

DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Naphcon A eye drops Recalled by Mckesson Medical-Surgical Inc. Corporate...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Bisacodyl Suppositories Recalled by Mckesson Medical-Surgical Inc. Corporate...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Systane Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due to...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Systane Balance Recalled by Mckesson Medical-Surgical Inc. Corporate Office...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Debrox Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due to...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: A&D Original Ointment Recalled by Mckesson Medical-Surgical Inc. Corporate...

The Issue: CGMP Deviations: products were stored outside the drug label specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Testosterone Gel 1% (25mg testosterone/2.5g of gel) 2.5 g per unit dose...

The Issue: Superpotent Drug: Out of specification assay result was obtained during...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 29, 2022· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Aspirin and Extended-Release Dipyridamole Capsules Recalled by Glenmark...

The Issue: Failed Tablet/Capsule Specification : Capsule breakage

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2022· Vi-Jon, LLC

Recalled Item: Hydrogen Peroxide Topical Solution USP Recalled by Vi-Jon, LLC Due to Cross...

The Issue: Cross Contamination With Other Products: Product is cross contaminated with...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Divalproex Sodium Delayed-Release Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: Failure occurred during routine stability...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Euphoria Capsules Recalled by Loud Muscle Science Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Marketed...

The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Euphoria Capsules Recalled by Loud Muscle Science Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 24, 2022· Vi-Jon, LLC

Recalled Item: Hydrogen Peroxide Topical Solution Recalled by Vi-Jon, LLC Due to Labeling:...

The Issue: Labeling: Label Mix-Up-The primary label on the front of the bottles have...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 24, 2022· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...

The Issue: Defective Delivery System: Customer complaints received for ripping patches...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: QP COUGH COLD TABLET 16 CT distributed to specific Family Recalled by Family...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: NPX ENEMA 4.5 FL OZ 2 PK distributed to specific Recalled by Family Dollar...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund