Biomet, Inc. Graft Preparation System, sterile, single use, disposable, Distributed by Biomet Biologics, Inc., Warsaw, Indiana; REF 800-0300. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Graft Preparation System, sterile, single use, disposable, Distributed by Biomet Biologics, Inc., Warsaw, Indiana; REF 800-0300.
Brand
Biomet, Inc.
Lot Codes / Batch Numbers
Lots 192180, exp. Jan 2012, 223260, exp. Jan 2012 and 652330, exp May 2011.
Products Sold
Lots 192180, exp. Jan 2012; 223260, exp. Jan 2012 and 652330, exp May 2011.
Biomet, Inc. is recalling Graft Preparation System, sterile, single use, disposable, Distributed by Biomet Biologics, Inc., Wa due to The syringe assembly has an obstruction in the tube that prevents the plunger from being depressed.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The syringe assembly has an obstruction in the tube that prevents the plunger from being depressed.
Recommended Action
Per FDA guidance
Consignees were notified by letter dated either 6/11/07 or 6/13/07 and requested to return the product.
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 noticePage updated: Jan 10, 2026