RecallRadar

FDA Drug recall D-0072-2022

ZEE+ painaid ESF Extra-Strength Formula (Acetaminophen 250 mg, Aspirin 250 mg (NSAID), Caffeine 65 mg) tablets, 2 Tablets per/package, Pack…

On 2021-11-03 the FDA classified a Class III recall of ZEE+ painaid ESF Extra-Strength Formula (Acetaminophen 250 mg, Aspirin 250 mg (NSAID), Caffeine 65 mg) tablets, 2 Tablets per/package, Pack… by Ultra Seal, citing failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0072-2022
ClassificationClass III
Statusterminated
Initiated2021-10-13
Published2021-11-03
Last updated2026-09-13 11:52 UTC
CompanyUltra Seal
DistributionUS

Product

ZEE+ painaid ESF Extra-Strength Formula (Acetaminophen 250 mg, Aspirin 250 mg (NSAID), Caffeine 65 mg) tablets, 2 Tablets per/package, Packaged in a) 50-count packages/carton, b) 125-count packages/carton, PA-ESF 1414Z, Dist. by: Zee Medical Distributors, LLC Mason, OH 45040 (Shipping Label)

Reason

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

Identifiers

code_infoLot #: AK-9547, exp. date 22- Apr; AK-9941, exp. date 22-Dec

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0072-2022%22

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