RecallRadar

FDA Drug recall D-0073-2022

AERO Tab PAIN RELIEVER (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets , 2 tablets Per Packet, Packaged in 10,000 Packets/Case…

On 2021-11-03 the FDA classified a Class III recall of AERO Tab PAIN RELIEVER (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets , 2 tablets Per Packet, Packaged in 10,000 Packets/Case… 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-0073-2022
ClassificationClass III
Statusterminated
Initiated2021-10-13
Published2021-11-03
Last updated2026-09-13 11:52 UTC
CompanyUltra Seal
DistributionUS

Product

AERO Tab PAIN RELIEVER (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets , 2 tablets Per Packet, Packaged in 10,000 Packets/Case, PO# 11938, Mfg. for: Aero Healthcare, Valley Cottage, NY 10989 (Shipping Label )

Reason

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

Identifiers

code_infoLot #: K-1278, exp. date 23-Jul; K-9371, AK-9463, exp. date 21-Nov; AK-9821, AK-9819, exp. date 22-Sep; 1107, exp. date 23-Mar.

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-0073-2022%22

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