FDA Medical Device Recalls (openFDA)
Bock,Otto,Orthopedic Ind,Inc: Modular Knee Joint with Friction Brake
- Recall number
- Z-1379-04
- Recalling firm
- Bock,Otto,Orthopedic Ind,Inc
- Product
- Modular Knee Joint with Friction Brake
- Status
- Terminated
- Initiated
- 2004-07-15
- Posted
- 2004-08-18
- Terminated
- 2005-11-07
- Reason
- Braking Plates of the 3R90 and 3R92 Modular Knee Joint with Friction Brake may become dislodged which may cause the braking performance of the knee to malfunction.
- Root cause
- Other
- Action
- The braking plate of the knee may become dislodged, which may cause the braking performance of the knee to malfunction.
- Quantity
- 457 devices
- Distribution
- not on file
- Lot, serial or model codes
- No lot numbers are used. Recall covers patients who were fit with either of the products between March 1, 2004 and July 9, 2004.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- ISH
- Firm FEI
- 2182293
- Firm city
- Minneapolis
- Firm state
- MN
- 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