FDA Medical Device Recalls (openFDA)
Zimmer Inc.: NexGen Complete Knee Solution Minimally Invasive Solutions MIS Technology Femoral Finishing Guide, instrumentation used in total knee arthroplasty procedures. Catalog No. 82015272522.
- Recall number
- Z-0651-2007
- Recalling firm
- Zimmer Inc.
- Product
- NexGen Complete Knee Solution Minimally Invasive Solutions MIS Technology Femoral Finishing Guide, instrumentation used in total knee arthroplasty procedures. Catalog No. 82015272522.
- Status
- Terminated
- Initiated
- 2006-10-10
- Posted
- 2007-03-28
- Terminated
- 2007-12-04
- Reason
- The device was cut to an incorrect angle, which may result in an incorrect bone cut.
- Root cause
- Other
- Action
- Product was removed from customer location during visit on 10/10/2006.
- Quantity
- 1
- Distribution
- One medical facility in Michigan.
- Lot, serial or model codes
- Lot 97000418.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JWH
- Firm FEI
- 1000220733
- Firm city
- Warsaw
- Firm state
- IN
- 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
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
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