Tri-Plex Adapter, single unit (MD-04000 )or box of 25 (MD-04001) or case of 100 (MD-04002). Sterile. Single Use.
FDA device recall Z-1371-05 · posted 2005-08-16 · Terminated
Recall details
- Recalling firm
- Medical Device Group Inc.
- Reason for recall
- Device separation presenting a choking hazard.
- Action taken
- Distributors were contacted by telephone on June 8, 2005, distributors were requested to return product. Letters were also sent by mail with proof of reciept on June 10, 2005. Firm reports that all customers have been notified.
- Root cause
- Other
- Status
- Terminated
- Product code
- MOD
- Quantity affected
- 2,282
- Distribution
- Nationwide, Brasil and Canada
- Date initiated
- 2005-06-08
- Date posted
- 2005-08-16
- Date terminated
- 2012-04-06
- Location
- Poway, CA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| TRI-PLEX ADAPTER (K010401) | The Medical Device Group, Inc. | 2002-10-30 |