AGA Gas Recalls Oxygen USP Due to GMP Deviations
AGA Gas Inc recalls 1,500 gallons of Oxygen USP bulk liquid due to cGMP deviations. Check lot numbers and distribution details.
Use caution until it’s fixed
cGMP Deviations; trailer may not have met GMP requirements prior to filling
Contact the company
What happened, in plain English
AGA Gas Inc is recalling Oxygen, USP, 99.0%, Bulk Cryogenic Liquid distributed in Ohio. The recall stems from cGMP deviations where the trailer may not have met Good Manufacturing Practice requirements prior to filling. No specific remedy or injury reports are listed in this record. Read more at govinfonow.com/recall/43350-aga-gas-inc-recalls-oxygen-usp-99-0-bulk-cryogenic.
Source Summary by GovInfoNow · govinfonow.com/recall/43350-aga-gas-inc-recalls-oxygen-usp-99-0-bulk-cryogenic · Updated October 11, 2026 · FDA enforcement record: FDA #D-0779-2016
Cite this page
“AGA Gas Recalls Oxygen USP Due to GMP Deviations.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/43350-aga-gas-inc-recalls-oxygen-usp-99-0-bulk-cryogenic. Based on FDA recall #D-0779-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0779-2016%22&limit=1).
Why it’s dangerous
The hazard is a potential failure in manufacturing standards, specifically that the trailer used for filling may not have met cGMP requirements. This could affect product quality or sterility, though the specific health consequences are not described in the record.
Who’s affected
Recipients of Oxygen, USP bulk liquid delivered to Ohio who possess Lot# 7931-O-V32-5330-5-1062. The record does not specify which medical conditions or users are most at risk.
How to tell if you have this one
Look for Oxygen, USP, 99.0%, Bulk Cryogenic Liquid with NDC 33237-001-01 and Lot# 7931-O-V32-5330-5-1062. The product was distributed to Ohio.
- Brand
AGA Gas- Category
Drug
What to do — step by step
Check Product Details
Verify if you have Oxygen, USP with NDC 33237-001-01 and Lot# 7931-O-V32-5330-5-1062.
Contact Manufacturer
Since the remedy is not stated in the record, contact AGA Gas Inc or Airgas Merchant Gases for instructions on how to proceed.
Where it went and when
Where it was distributed
Distributed in Ohio.
FDA distribution: “Product was delivered to Ohio” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Ohio.
Recall timeline
FDA terminated this recall 2 years 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-0779-2016 (November 29, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0779-2016 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.