FDA Medical Device Recalls (openFDA)
Wright Medical Technology Inc: Achillon minimally invasive Achilles tendon suture system
- Recall number
- Z-1304-04
- Recalling firm
- Wright Medical Technology Inc
- Product
- Achillon minimally invasive Achilles tendon suture system
- Status
- Terminated
- Initiated
- 2004-07-02
- Posted
- 2004-07-31
- Terminated
- 2005-07-05
- Reason
- Lack of sterility assurance
- Root cause
- Other
- Action
- Wright Medical Technology notified its consignees via email and telephone to ensure that the email was received. The consignees asked to return any in-stock recalled product to Wright Medical Technology.
- Quantity
- 20 units
- Distribution
- Nationwide
- Lot, serial or model codes
- Product: Achillon Reference No.: 119 700 Batch No.: C Sterilization Batch No.: S037
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- MCZ
- Firm FEI
- 1043534
- Firm city
- Arlington
- Firm state
- TN
- 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