FDA Medical Device Recalls (openFDA)
Alpha-Omega Services Inc: Template Needle, Series 17, 20 cm, with Threaded Female hub and Bent Stylet, Closed-End, Disposable. Packaged in single, 10, 15, 20 per package.
- Recall number
- Z-0570-04
- Recalling firm
- Alpha-Omega Services Inc
- Product
- Template Needle, Series 17, 20 cm, with Threaded Female hub and Bent Stylet, Closed-End, Disposable. Packaged in single, 10, 15, 20 per package.
- Status
- Terminated
- Initiated
- 2003-09-04
- Posted
- 2004-07-20
- Terminated
- 2004-04-29
- Reason
- Template needle may fracture leaving tip in patient.
- Root cause
- Other
- Action
- A fax of the recall notice was made on 9/4/2003 and a follow-up telephone call was made. This recall is complete.
- Quantity
- 1330
- Distribution
- LA, MN, CA, VA, CO, TX, ID, NY, KS, WA
- Lot, serial or model codes
- Lots F01068, F01099, F01100, F01128.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- MIJ
- Firm FEI
- 2022694
- Firm city
- Bellflower
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28