HF Acquisition Co. LLC recalls Famotidine Injection, USP, 20 mg/2mL, 2 mL vial, Rx only, Single Dose Vial, For Intravenous Use Only After Dilution,
HF Acquisition Co recalls Famotidine injection vials due to temperature abuse complaints. Product received non-refrigerated, risking safety.
Lower-risk recall
TEMPERATURE ABUSE: Complaint received from customer that product was received in a non-refrigerated state.
Contact the company & request your remedy
What happened, in plain English
HF Acquisition Co. recalls Famotidine injection vials because customers reported receiving them without refrigeration. This could lead to unsafe conditions if the product is not stored properly. Read more at govinfonow.com/recall/37042-hf-acquisition-co-recalls-famotidine-injection-temperature-abuse-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/37042-hf-acquisition-co-recalls-famotidine-injection-temperature-abuse-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1392-2020
Cite this page
“HF Acquisition Co recalls Famotidine injection: Temperature abuse risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37042-hf-acquisition-co-recalls-famotidine-injection-temperature-abuse-risk. Based on FDA recall #D-1392-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1392-2020%22&limit=1).
Why it’s dangerous
The product was reported to be received in a non-refrigerated state. This temperature abuse could affect the product's safety and effectiveness.
Who’s affected
Prescription patients using Famotidine injection vials. Those who received the vials without refrigeration are most at risk.
How to tell if you have this one
Check for vials labeled 'Famotidine Injection, USP, 20 mg/2mL, 2 mL vial, Rx only'. The product was distributed by HF Acquisition Co, LLC with NDC 63323-739-12 and Lot #6122639.
- Brand
HF Acquisition Co- Category
Drug
What to do — step by step
Check Storage Conditions
Ensure the vial has been stored in refrigeration since receipt.
Questions people ask
Is this product safe if stored properly?
The recall is due to temperature abuse complaints, not inherent safety issues. Proper refrigeration should ensure safety.
What should I do if I have this product?
The recall does not specify a remedy, so check storage conditions and contact your healthcare provider for guidance.
How can I tell if I have the recalled product?
Look for vials labeled 'Famotidine Injection, USP, 20 mg/2mL, 2 mL vial, Rx only' with NDC 63323-739-12 and Lot #6122639.
Contact HF Acquisition Co
We’ve drafted a message you can send HF Acquisition Co to request your refund or repair — edit it as you like.
Subject: Recall D-1392-2020 — HF Acquisition Co HF Acquisition Co Hello, I own a HF Acquisition Co that is covered by recall D-1392-2020 from HF Acquisition Co. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1392-2020 (June 17, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1392-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.