MurphyScope, Bayonet, Malleable, Catalog # 2121-157
FDA device recall Z-0615-05 · posted 2005-03-12 · Terminated
Recall details
- Recalling firm
- Medtronic Neurosurgery
- Reason for recall
- Products are mislabeled.
- Action taken
- Recall letters were sent to customers on 2/28/05 requesting return for replacement.
- Root cause
- Process control
- Status
- Terminated
- Product code
- GWG
- Quantity affected
- 2
- Distribution
- NJ and India.
- Date initiated
- 2005-02-28
- Date posted
- 2005-03-12
- Date terminated
- 2005-07-12
- Location
- Goleta, CA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| MEDTRONIC PS MEDICAL MURPHYSCOPE, MODELS 2125-032, 2125033,2125-042, 2125-043, 2125-157, 2125-158,2125-161 2125-162,, (K010341) | Medtronic PS Medical | 2001-04-20 |