Femoral Sponge 10 inches REF 206-715, Rx Sterile, Stryker Instruments Kalamazoo, MI. The femoral sponge is an absorbent that is used to dry the intramedullary canal prior to the application of bone cement. The suction effectively absorbs blood and fluid from the canal. It may provide swabbing/scrubbing action during suction.
This recall has been terminated (originally issued March 15, 2010).
- Recall Initiated
- January 25, 2010
- Posted
- March 15, 2010
- Terminated
- October 25, 2010
- Recall Number
- Z-1104-2010
- Quantity
- 9,257 all products
- Firm Location
- Kalamazoo, MI
- Official Source
- View on FDA website ↗
Reason for Recall
The firm did not have packaging validation to support the labeled shelf life. There is potential for a breach in sterility specific to the sterile packaged femoral sponge which may result in a non-sterile product.
Distribution
Worldwide Distribution -- United States, Canada, Mexico, Australia, Brazil, Switzerland, Japan, Netherlands, England, UK, Sweden, Hong Kong, Korea, Malaysia, Singapore, Argentina, Spain, and Italy.
Lot / Code Info
743288, 743289, 743330, 743331, 743332, 743333, 743362, 743363, 743364, 743365, 743378, 743379, 743380, 743381, 743390, 743391, 743400, 743402, 743403, 743404, 743405, 743418, 743419, 743420, 743421, 743422, 743423, 743445, 743446, 743447, 743448 and 743449.
Root Cause
Other
Action Taken
A "Medical Device Recall Notification" dated January 21, 2010 was issued to customers. The notification described the affected product, issue and actions to take. Consignees were asked to forward the notification to all their affected locations. Customers were instructed to immediately check inventory and quarantine any recalled product found. Consignees were instructed to destroy all product and report how much product was destroyed. For questions regarding this recall, please contact Stryker Instruments by calling 1-800-800-4236, ext. 4354