Oklahoma Respiratory Care Recalls Compressed Oxygen Cylinders for Purity Failures
Oklahoma Respiratory Care Inc. is recalling 94 cylinders of compressed oxygen in Oklahoma because purity readings were out of specification.
The agency’s classification
FDA (Drugs): Class II
Class II is 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.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses or injuries, fitting the criteria for a moderate severity score.
Plain-English summary
Oklahoma Respiratory Care Inc. is recalling 94 cylinders of Oxygen, Compressed USP UN1072 Medical Gas. The product is supplied in 682-liter and 165-liter cylinders and is available by prescription only. The recall covers lot numbers 03141201, 03211201, 05021201, 06271201, and 11081201.
The recall was initiated because purity readings for the oxygen were out of specification, failing impurities and degradation requirements. The affected products were distributed in Oklahoma.
Consumers with this product should contact Oklahoma Respiratory Care at 800.262.9857 for instructions on how to proceed.
The recalled product
- Product
- Oxygen, Compressed USP UN1072 Medical Gas supplied in a) 682 litres and b)165 litres cylinders, Rx only, Oklahoma Respiratory Care 800.262.9857, Norman, OK 73071
- Manufacturer
- Oklahoma Respiratory Care Inc
- Category
- Drug — Medical Gas
- Hazard
- Affected units
- 94
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (5)
- Lot numbers: 03141201
- 03211201
- 05021201
- 06271201
- and 11081201.
Distribution
Distributed in 1 state:
Related recalls
Same manufacturer · Oklahoma Respiratory Care Inc
See all →- ModerateOklahoma Respiratory Care Recalls Compressed Oxygen Cylinders for Testing Failures
FDA (Drugs) · 2012-08-15
Other drug recalls
- SevereK.C. Pharmaceuticals Recalls Target Eye Drops for Sterility Concerns
FDA (Drugs) · 2026-10-14
- SevereFDA Recalls Tirzepatide Injectable Due to Sterility Concerns
FDA (Drugs) · 2026-10-14
- SevereFDA Recalls Semaglutide/Cyanocobalamin Injectable Due to Sterility Concerns
FDA (Drugs) · 2026-10-14
- LowSun Pharmaceutical Recalls Tretinoin Cream Due to Impurity Failures
FDA (Drugs) · 2026-10-14
- SevereK.C. Pharmaceuticals Recalls Leader Advanced Relief Eye Drops for Sterility Concerns
FDA (Drugs) · 2026-10-14
Similar recalls
- ModerateOklahoma Respiratory Care Recalls Compressed Oxygen Cylinders for Testing Failures
FDA (Drugs) · 2012-08-15
- LowMedical Park Homecare Recalls Compressed Oxygen Cylinders Due to Gauge Issues
FDA (Drugs) · 2016-03-23
- HighCompressed Oxygen Cylinders Recalled Due to Manufacturing Quality Deviations
FDA (Drugs) · 2023-11-22
- ModerateAirgas Recalls 145 Compressed Oxygen Cylinders Due to Short Fill Error
FDA (Drugs) · 2014-01-01
- ModerateLinde Recalls 283 Oxygen Cylinders Due to Calibration Deviations
FDA (Drugs) · 2012-06-27
- HighGrace Healthcare Recalls Compressed Oxygen Cylinders Due to Manufacturing Deviations
FDA (Drugs) · 2021-05-05