AtHome Medical Oxygen Refrigerated Liquid Recall: GMP Testing Issue
AtHome Medical recalls oxygen refrigerated liquid (Rx only) due to lack of SOP for testing out of specifications. This may affect safety in medical use. Contact for details.
Lower-risk recall
GMP Deviations: The firm does not include an SOP for testing for out of specifications.
Contact the company
What happened, in plain English
AtHome Medical is recalling oxygen refrigerated liquid (Rx only) because their manufacturing process didn't have a standard procedure for testing when products go out of specifications. This could lead to unsafe medical use if the oxygen isn't properly tested. Read more at govinfonow.com/recall/41625-athome-medical-oxygen-refrigerated-liquid-recall-gmp-testing-issue.
Source Summary by GovInfoNow · govinfonow.com/recall/41625-athome-medical-oxygen-refrigerated-liquid-recall-gmp-testing-issue · Updated October 8, 2026 · FDA enforcement record: FDA #D-1060-2017
Cite this page
“AtHome Medical Oxygen Refrigerated Liquid Recall: GMP Testing Issue.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/41625-athome-medical-oxygen-refrigerated-liquid-recall-gmp-testing-issue. Based on FDA recall #D-1060-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1060-2017%22&limit=1).
Why it’s dangerous
The product was made without a standard operating procedure (SOP) for testing when it goes out of specifications. This means the oxygen might not be safe for medical use if it doesn't meet quality standards.
Who’s affected
People with prescriptions for oxygen refrigerated liquid from AtHome Medical are affected. Those using this product for medical purposes are at risk if the testing process was inadequate.
How to tell if you have this one
Check for the product name 'Oxygen Refrigerated Liquid USP UN 1073' with prescription status. Look for lot number 051017V1 and expiration date 5/11/17.
- Brand
AtHome Medical- Category
Drug
What to do — step by step
Check Product Details
Verify the lot number and expiration date on the product label.
Where it went and when
Where it was distributed
Distributed in New Jersey.
FDA distribution: “NJ” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: New Jersey.
Recall timeline
FDA terminated this recall 11 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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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-1060-2017 (May 11, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1060-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.