RecallDepth

PROLENE* Mesh, Polypropylene Non Absorbable Synthetic Surgical Mesh, PMII, 3''x6'', each mesh in a sealed pouch package, 6 packages per papercard carton. Cartons labeled in part ***ETHICON, INC., a Johnson & Johnson company SOMERVILLE, NEW JERSEY 08876-0151 ***STERILE: Sterility of contents guaranteed unless package has been opened or damaged***

This recall has been terminated (originally issued December 18, 2003).

Company
Owens & Minor Distribution, Inc.
Recall Initiated
November 3, 2003
Posted
December 18, 2003
Terminated
August 4, 2011
Recall Number
Z-0251-04
Quantity
CANNOT BE DETERMINED
Firm Location
Allen, VA
Official Source
View on FDA website ↗

Reason for Recall

Counterfeit product is an unapproved medical device with associated potential health hazard.

Distribution

Counterfeit and authentic product was distributed to warehouses and 205 medical facilities nationwide.

Lot / Code Info

Lots RBE609 EXP 1/07, RJJ130 EXP7/07

Root Cause

Other

Action Taken

The distributor notified the firm's chain of warehouses by e-mail on 10/31/03 to identify, segregate and quarantine potential counterfeit product. The distributor then notified consignees by letter on 11/3/03. The letter advised that customers may have received 2 lots of counterfeit product and described the features for identity, which were provided by the manufacturer (www.ethicon.com) of the authentic product. The notification further instructed that appropriate healthcare professionals should be advised of the recall. Consignees were instructed to quarantine the specified lots for return.