Template Needle, Series 17, 20 cm, with Threaded Female hub and Bent Stylet, Closed-End, Disposable. Packaged in single,
FDA device recall Z-0570-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Alpha-Omega Services Inc
- Reason for recall
- Template needle may fracture leaving tip in patient.
- Action taken
- A fax of the recall notice was made on 9/4/2003 and a follow-up telephone call was made. This recall is complete.
- Root cause
- Other
- Status
- Terminated
- Product code
- MIJ
- Quantity affected
- 1330
- Distribution
- LA, MN, CA, VA, CO, TX, ID, NY, KS, WA
- Date initiated
- 2003-09-04
- Date posted
- 2004-07-20
- Date terminated
- 2004-04-29
- Location
- Bellflower, CA
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