Home › NINGBO MAXCON MEDICAL TECHNOLOGY CO., LTD. › Maxcon Sharps container
Maxcon Sharps container
NINGBO MAXCON MEDICAL TECHNOLOGY CO., LTD. · Model MA1421 · UDI-DI 06970623201419
1
510(k) clearances
982
Adverse events (2 deaths)
3
Recalls
95
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-08-23 | Bemis Health Care,Inc | The 5 Quart Wall Safes are shipped as two pieces (bottom & top) that customers are unable to assemble because of excess warp in the back wall of the container. |
| 2006-04-03 | EM Innovations Inc | The firm failed to include User Instructions with the Stic Kit Needle Containment Device, Model EMI 82691, which they shipped to distributor/customers. |
| 2004-02-25 | Bemis Manufacturing Co. | The closure flap of the recalled sharps containers have two tabs that fit into slots on the cover for final closure and locking but some of the covers have one of the tabs that wil |
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 docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.