Afassco Pain Free Plus X-STRENGTH PAIN RELIEVER (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 Tablets/package, Packaged in 12,000 Packets/Case, PO# 19540, Mfg. for: Afassco Minden, NV 89423 (Shipping Label)

Class I - Dangerous
💊 Drugs Recalled: October 13, 2021 Ultra Seal Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot #: 9819, K-9819, exp. date 22-Sep
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Ultra Seal Corporation
Reason for Recall:
Failed Stability Specifications: Out-of-Specification results observed for Aspirin related compound Salicylic Acid.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Afassco Pain Free Plus X-STRENGTH PAIN RELIEVER (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 Tablets/package, Packaged in 12,000 Packets/Case, PO# 19540, Mfg. for: Afassco Minden, NV 89423 (Shipping Label)

Product Codes/Lot Numbers:

Lot #: 9819, K-9819, exp. date 22-Sep

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0077-2022

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