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Class III: unlikely to cause harmTerminated

Ultra Seal AERO Tab PAIN RELIEVER Recall

AERO Tab PAIN RELIEVER (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets , 2…

Ultra Seal Corporation · New Paltz, NY

Risk level
Class III
Reported by FDA
Nov 3, 2021
Recall ID
D-0073-2022
Check your lot numberHow we source this data

Summary

Ultra Seal recalled AERO Tab PAIN RELIEVER starting Oct 13, 2021. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0073-2022 on Nov 3, 2021. Reason: Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid. Status: Terminated.

Why it was recalled

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

Product description

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 )

Lot numbers, UPCs & expiration codes

Lot #: 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.

Where it was sold

Nationwide in the USA.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0073-2022
Classification
Class III
Status
Terminated
Recall initiated
Oct 13, 2021
FDA report date
Nov 3, 2021
Quantity
1,480,981 tablets
Recall type
Voluntary: Firm initiated
Recalling firm
Ultra Seal Corporation

Original FDA data

Every field from FDA enforcement report D-0073-2022, exactly as published.

Show all FDA fields
City
New Paltz
State
NY
Status
Terminated
Country
United States
Event ID
88843
Address
521 Main St
Code information
Lot #: 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.
Postal code
12561-1609
Report date
Nov 3, 2021
Product type
Drugs
Recall number
D-0073-2022
Classification
Class III
Recalling firm
Ultra Seal Corporation
Product quantity
1,480,981 tablets
Termination date
Mar 28, 2022
Reason for recall
Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
Voluntary / mandated
Voluntary: Firm initiated
Product description
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 )
Distribution pattern
Nationwide in the USA.
Recall initiation date
Oct 13, 2021
Initial firm notification
Letter
Center classification date
Oct 26, 2021

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0073-2022, published Nov 3, 2021. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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