Oxygen Compressed Gas (Oklahoma Respiratory) – CGMP Testing Issues (2012)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
OXYGEN, COMPRESSED USP MEDICAL GAS in the following containers: E Cylinder 680L, D Cylinder 425L, and M6 Cylinder 165L, Rx only, Oklahoma Respiratory Care, Norman, OK
Brand
Oklahoma Respiratory Care Inc
Lot Codes / Batch Numbers
All lots distributed January 1, 2011 - October 18, 2011.
Products Sold
All lots distributed January 1, 2011 - October 18, 2011.
Oklahoma Respiratory Care Inc is recalling OXYGEN, COMPRESSED USP MEDICAL GAS in the following containers: E Cylinder 680L, D Cylinder 425L, a due to CGMP Deviations; no identity or purity testing on incoming oxygen gas, and lack of documentation. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA drug enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
CGMP Deviations; no identity or purity testing on incoming oxygen gas, and lack of documentation
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm, their healthcare provider, or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
OK
Page updated: Jan 7, 2026