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
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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.
Brand
Zimmer Inc.
Lot Codes / Batch Numbers
Lots 480103, 480104 and 487665.
Products Sold
Lots 480103, 480104 and 487665.
Zimmer Inc. is recalling Zimmer brand Sirus Intramedullary femur nail system step reamer 0 mm, 6.5/4.5 mm cannulated, for cer due to The calibrations on the reamers may lead to inaccurate reaming depth when used in accordance with the published surgical technique.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The calibrations on the reamers may lead to inaccurate reaming depth when used in accordance with the published surgical technique.
Recommended Action
Per FDA guidance
Consignees were notified via recall letter dated 9/30/05.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, CA, FL, GA, IL, IN, KS, MI, MN, NJ, NY, NC, OH, OR, PA, TN, TX, UT, VA
Page updated: Jan 10, 2026