Biomet Microfixation, Inc. Fredrick's Converse Retractor #5 F/O, Model Number: 01-0485. A fiber optic retractor used in plastic surgery procedures to retract tissue. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Fredrick's Converse Retractor #5 F/O, Model Number: 01-0485. A fiber optic retractor used in plastic surgery procedures to retract tissue.
Brand
Biomet Microfixation, Inc.
Lot Codes / Batch Numbers
Lot # 042408D08
Products Sold
Lot # 042408D08
Biomet Microfixation, Inc. is recalling Fredrick's Converse Retractor #5 F/O, Model Number: 01-0485. A fiber optic retractor used in plasti due to Fiber optic cable is missing from the Frederick's Converse Retractor Lot # 042408D08.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Fiber optic cable is missing from the Frederick's Converse Retractor Lot # 042408D08.
Recommended Action
Per FDA guidance
Consignee was notified by certified mail via an Urgent Medical Device Recall Notice dated 10/24/08, with return receipt. The letter identifies the product and states the issue with the product. The letter required the customer to discontinue use of the item and return it to Biomet Microfixation so that they may rework the instrument. It also asked the customer to notify any hospital personnel responsible for receiving recall notices of this action if the product had been further distributed. The RGA number should be utilized to return the products. The Inventory Reconciliation sheet should be filled out and faxed to 904-741-9425.
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