FDA Medical Device Recalls (openFDA)
Immedica Inc: TransFx Pin, External Fixation Pin. 3.0 /4.0 mm x 80mm, 20mm thread.
- Recall number
- Z-0907-03
- Recalling firm
- Immedica Inc
- Product
- TransFx Pin, External Fixation Pin. 3.0 /4.0 mm x 80mm, 20mm thread.
- Status
- Terminated
- Initiated
- 2003-02-10
- Posted
- 2003-06-05
- Terminated
- 2003-10-09
- Reason
- Mislabeled; wrong identification number on pin.
- Root cause
- Other
- Action
- Recall letter was sent on 2/10/2003 to Zimmer Patient Care Division. The letter states that Zimmer is to conduct a sub-recall to their customers to account for the 127 pieces sent to them.
- Quantity
- 127
- Distribution
- The product is only distributed to Zimmers Patient Care Division, P.O. Box 569, Dover, OH 44622. There are no government accounts.
- Lot, serial or model codes
- Catalog No./Part No./Ref.No. -- 00-4453-34-08. Lot Number: 70209800
- 510(k) numbers
- ["K990848"]
- PMA numbers
- not on file
- Product code
- LXT
- Firm FEI
- 1000222312
- Firm city
- Chatham
- Firm state
- NJ
- 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