Un1002 Air recalls
The FDA has published 2 recalls involving Un1002 Air since 2016. The latest was reported on 6 Apr 2016. Most were for manufacturing (cgmp) deviations. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls2since 2016
Last 12 months0reported
Class I00% of total
Ongoing0latest 6 Apr 2016
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 0 0%Class III 2 100%
Why un1002 air is recalled
Companies
By year
All un1002 air recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | UN1002 Air, Compressed, Breathing Grade recalled by Praxair | Praxair | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | UN1002 Air, Compressed, Medical Air recalled by Praxair | Praxair | Manufacturing (CGMP) Deviations | Nationwide |
Should you stop taking Un1002 Air?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.