Biomet, Inc. Vortech Graft Preparation System, sterile, single use, disposable, Distributed by Biomet Biologics, Inc., Warsaw, Indiana; REF 800-0300V. (Not sold in the United States). Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Vortech Graft Preparation System, sterile, single use, disposable, Distributed by Biomet Biologics, Inc., Warsaw, Indiana; REF 800-0300V. (Not sold in the United States).
Brand
Biomet, Inc.
Lot Codes / Batch Numbers
Lot 192380, exp. Jan 2012.
Products Sold
Lot 192380, exp. Jan 2012.
Biomet, Inc. is recalling Vortech Graft Preparation System, sterile, single use, disposable, Distributed by Biomet Biologics, 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