Zimmer brand Sirus Intramedullary femur nail system step reamer 0 mm, 6.5/4.5 mm cannulated, for cervical screws, item n
FDA device recall Z-0091-06 · posted 2005-10-28 · Terminated
Recall details
- Recalling firm
- Zimmer Inc.
- Reason for recall
- The calibrations on the reamers may lead to inaccurate reaming depth when used in accordance with the published surgical technique.
- Action taken
- Consignees were notified via recall letter dated 9/30/05.
- Root cause
- Other
- Status
- Terminated
- Product code
- GFG
- Quantity affected
- 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.
- Date initiated
- 2005-09-30
- Date posted
- 2005-10-28
- Date terminated
- 2005-12-28
- Location
- Warsaw, IN
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