Drug recall
LifeGas OXYGEN COMPRESSED UN1072 USP, Distributed by: Linde
FDA recall event 61917 · Class II · Linde Gas LLC
Key facts
| Event ID | 61917 |
|---|---|
| Recall numbers | D-1383-2012 |
| Recalling firm | Linde Gas LLC |
| Product type | Drugs |
| Products | LifeGas OXYGEN COMPRESSED UN1072 USP, Distributed by: Linde |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | CGMP Deviations: The pressure gages, vacuum gages, and thermometer had surpassed the calibration expiry period, which may have resulted in overfill/underfill of oxygen cylinders. |
| Initiation date | May 4, 2012 |
| Report date | Jun 27, 2012 |
| Termination date | Jun 11, 2013 |
| City | Columbus |
| State | OH |
| Country | United States |
| FEI number | 3003723008 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: