Boehringer Suction Regulator Model number 3714
FDA device recall Z-0157-06 · posted 2005-11-17 · Terminated
Recall details
- Recalling firm
- Boehringer Laboratories, Inc.
- Reason for recall
- Condition exists that prevents complete shutoff of the valve
- Action taken
- The recalling firm telephoned their customers on 7/25/05 to inform them of the problem, request the return of the recalled product, and inform them that replacement products were being shipped
- Root cause
- Other
- Status
- Terminated
- Product code
- KDP
- Quantity affected
- 1829 units
- Distribution
- The products were shipped to hospitals AZ, AK, CA, FL, LA, MI, MO, NC, NJ, OR, PA, SC, UT, VA, and WA.
- Date initiated
- 2005-08-01
- Date posted
- 2005-11-17
- Date terminated
- 2005-11-16
- Location
- Norristown, PA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| BOEHRINGER LABORATORIES SUCTION INTERMITTOR (K853095) | Boehringer Laboratories | 1985-08-23 |