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Ultra Seal Corporation recalls Vica-Cet BACK PAIN RELIEF (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 tablets/pk, packaged in 10,000

Recalled November 3, 2021 · FDA recall D-0071-2022 · Ultra Seal

Hazard
Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid. · FDA Class III
Units
1,367,525 tablets
Sold at
Nationwide in the USA.

Description

Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.

Product
Vica-Cet BACK PAIN RELIEF (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 tablets/pk, packaged in 10,000 packets, PO# 8967, Mfg. for Tellus/The Provision First Aid Line (Shipping Label)
Manufacturer(s)
Ultra Seal Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Ultra Seal Corporation recalls Vica-Cet BACK PAIN RELIEF (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 tablets/pk, packaged in 10,000 | RecallWatchUSA