FDA Medical Device Recalls (openFDA)
Zimmer Inc.: Zimmer brand Sirus Intramedullary femur nail system step reamer 0 mm, 6.5/4.5 mm cannulated, for cervical screws, item number 02.00020.039.
- Recall number
- Z-0091-06
- Recalling firm
- Zimmer Inc.
- Product
- Zimmer brand Sirus Intramedullary femur nail system step reamer 0 mm, 6.5/4.5 mm cannulated, for cervical screws, item number 02.00020.039.
- Status
- Terminated
- Initiated
- 2005-09-30
- Posted
- 2005-10-28
- Terminated
- 2005-12-28
- Reason
- The calibrations on the reamers may lead to inaccurate reaming depth when used in accordance with the published surgical technique.
- Root cause
- Other
- Action
- Consignees were notified via recall letter dated 9/30/05.
- Quantity
- 27
- Distribution
- Arizona, California, Florida, Georgia, Illinois, Indiana, Kansas, Michigan, Minnesota, New Jersey, New York, North Carolina, Ohio, Oregon, Pennsylvania, Tennessee, Texas, Utah and Virginia.
- Lot, serial or model codes
- Lots 480103, 480104 and 487665.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- GFG
- 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
- 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