Famotidine Injection recall
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
Why was Famotidine Injection recalled?
TEMPERATURE ABUSE: Complaint received from customer that product was received in a non-refrigerated state.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 6122639, Exp. Date 08/2021
- Product
- 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
- Recalling firm
- HF Acquisition Co. LLC
- Quantity
- N/A
- Distribution
- The vials were distributed to one consignee located in CT.
- Recall date
- July 29, 2020
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)