Famotidine Injection, USP, 20 mg/2mL, 2 mL vial, Rx only, Single Dose Vial, For Intravenous Use Only After Dilution, Distributed by HF Acquisition Co, LLC, Mukilteo, WA 98275, NDC 63323-739-12
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot #: 6122639, Exp. Date 08/2021
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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:
- TEMPERATURE ABUSE: Complaint received from customer that product was received in a non-refrigerated state.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Famotidine Injection, USP, 20 mg/2mL, 2 mL vial, Rx only, Single Dose Vial, For Intravenous Use Only After Dilution, Distributed by HF Acquisition Co, LLC, Mukilteo, WA 98275, NDC 63323-739-12
Product Codes/Lot Numbers:
Lot #: 6122639, Exp. Date 08/2021
Distribution:
Distributed in: CT
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-1392-2020
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