PlainRecalls
FDA Drug Low Class III Terminated

Atropine Sulfate Ophthalmic Solution, USP 1%, 5 mL bottles, Rx only, Manufactured for: Somerset Therapeutics, LLC. Somerset, NJ 08873, NDC 70069-716-01

Reported: January 8, 2025 Initiated: December 16, 2024 #D-0169-2025

Product Description

Atropine Sulfate Ophthalmic Solution, USP 1%, 5 mL bottles, Rx only, Manufactured for: Somerset Therapeutics, LLC. Somerset, NJ 08873, NDC 70069-716-01

Reason for Recall

Failed Impurities/Degradation Specifications

Details

Recalling Firm
SOMERSET THERAPEUTICS LLC
Units Affected
5,870 bottles
Distribution
Nationwide within the United States
Location
Somerset, NJ

Frequently Asked Questions

What product was recalled?
Atropine Sulfate Ophthalmic Solution, USP 1%, 5 mL bottles, Rx only, Manufactured for: Somerset Therapeutics, LLC. Somerset, NJ 08873, NDC 70069-716-01. Recalled by SOMERSET THERAPEUTICS LLC. Units affected: 5,870 bottles.
Why was this product recalled?
Failed Impurities/Degradation Specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on January 8, 2025. Severity: Low. Recall number: D-0169-2025.