RecallDepth

***REF C9944A***"FULL RADIUS RESECTOR"***2.9mm***Qty 6***STERLING***STERILE***Rx Only.*** Made in the USA***Manufacturer: CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA***ConMed Linvatec Biomaterials, Ltd.Hermiankatu 6-8L 33720 Tampere, FINLAND.***Lot number # 95987. Soft Tissue resection and removal.

This recall has been terminated (originally issued February 10, 2012).

Company
Linvatec Corp. Dba Conmed Linvatec
Recall Initiated
November 12, 2009
Posted
February 10, 2012
Terminated
February 13, 2012
Recall Number
Z-0987-2012
Quantity
30 Units
Firm Location
Largo, FL
Official Source
View on FDA website ↗

Reason for Recall

ConMed Linvatec, Largo, FL recalled catalog number, C9944A, lot # 95987, 2.9MM Full Radius Resector Blade in November 2009 because there was a possibility that the device was assembled with an incorrect outer tube.

Distribution

Product Distributed in the states of Georgia and New York.

Lot / Code Info

Lot # 95987

Root Cause

Employee error

Action Taken

A Linvatec Corporation dba ConMed Linvatec sales representative contacted the affected customers by telephone on November 12, 2009. The customers were also contacted by the Recall Coordinator. The product, problem, and action to be taken by the customers were discussed. Customers with the product in their inventory were instructed to return the product to the firm. Contact the firm at 727-399-5205 for questions regarding this recall.

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