Home › Device types › OIG
Powder-Free Guayle Rubber Examination Glove
FDA product code OIG · Class 1 · General Hospital
0
Registered devices
2
Adverse events
2
Recalls
1
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-02-03 | Medline Industries Inc | The recall was initiated because the affected lot, lot number JCU004958569, of gloves did not meet the requirements for the water-leak test. |
| 2011-02-03 | Medline Industries Inc | The recall was initiated because the affected lot, lot number JCU004958569, of gloves did not meet the requirements for the water-leak test. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
