Stryker brand Birthing Bed; Model 4701.
FDA device recall Z-0793-05 · posted 2005-05-03 · Terminated
Recall details
- Recalling firm
- Stryker Medical
- Reason for recall
- Trendelenburg and reverse trendelenburg features may not function.
- Action taken
- Consignees were notified via letter dated 3/31/05 and Stryker personnel began visiting the facilities to make corrections.
- Root cause
- Other
- Status
- Terminated
- Product code
- HDD
- Quantity affected
- 31
- Distribution
- California, Georgia, Indiana, Iowa, Michigan, Ohio and Pennsylvania.
- Date initiated
- 2005-03-31
- Date posted
- 2005-05-03
- Date terminated
- 2005-05-09
- Location
- Kalamazoo, MI
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| ADEL 5000 (K950889) | Stryker Corp. | 1995-10-16 |