🔍 RecallPedia

GLYCOPYRROLATE INJECTION, USP 0.2MG/ML, 1mL VIAL, manufactured by HF Acquisition Co. LLC, Mukilteo, WA 98275, NDC 51662-1487-3

Class I - Dangerous
💊 Drugs Recalled: June 6, 2023 HF Acquisition Co Prescription Drugs

What Should You Do?

  1. Check if you have this product:
    Lot #: 2205095.1, Exp. Date 7/31/2024
  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:
HF Acquisition Co LLC
Reason for Recall:
Labeling: Label Mix-up
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

GLYCOPYRROLATE INJECTION, USP 0.2MG/ML, 1mL VIAL, manufactured by HF Acquisition Co. LLC, Mukilteo, WA 98275, NDC 51662-1487-3

Product Codes/Lot Numbers:

Lot #: 2205095.1, Exp. Date 7/31/2024

Distribution:

Distributed in: TX, AZ, CA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0870-2023

Related Recalls