FDA Medical Device Recalls (openFDA)
Plus Orthopedics USA: Plus Orthopedics Gliding Nail 17mm proximal / 11mm distal, 125 degrees, 180mm; Model Number: 0132073, Plus Orthopedics USA, San Diego, CA 92121
- Recall number
- Z-0360-2008
- Recalling firm
- Plus Orthopedics USA
- Product
- Plus Orthopedics Gliding Nail 17mm proximal / 11mm distal, 125 degrees, 180mm; Model Number: 0132073, Plus Orthopedics USA, San Diego, CA 92121
- Status
- Terminated
- Initiated
- 2003-06-30
- Posted
- 2007-12-08
- Terminated
- 2007-12-13
- Reason
- The device was produced without the required distal locking hole
- Root cause
- Reprocessing Controls
- Action
- The initial depth of the withdrawal action taken in June, 2003 ,was to the distributor (agent) level. Plus USA contacted individual agent sites showing inventory of the affected article numbers on hand and requested that those items be returned to Plus USA.
- Quantity
- 3
- Distribution
- Nationwide: AZ and ID
- Lot, serial or model codes
- Model Number: 0132073, Lot Number : 024332
- 510(k) numbers
- K020240
- PMA numbers
- not on file
- Product code
- KTT
- Firm FEI
- 3001237832
- Firm city
- San Diego
- 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