ClearanceBrief
Recall Z-1136-04 ยท KKX Drape, Surgical, Antimicrobial

Medikmark, Incorporated

Staple Removal Tray/Set/Kit; a sterile Rx convenience kit containing a staple remover instrument, an alcohol prep pad, a PVP prep pad and a gauze sponge. Theses kits were marketed under the following labels, 50 kits per case: a) Medikmark inc. Staple Removal Tray, reorder no. RS-2000, 3600 Bur Wood Drive, Waukegan, IL 60085; b)Medikmark Inc. Staple Removal Set, reorder no. SR-2000; 3600 Bur Wood

DateJul 22, 2004 (initiated Jul 12, 2004)
StatusTerminated
ReasonThe tip of the staple remover may puncture a hole in the wall of the tray, compromising the sterility of the kit.
Root causeOther
ActionRecall notifications were sent by fax and follow-up registered mail to the direct account distributors and users on 7/12-15/04. The accounts were informed of the potential non-sterility of the product and were instructed to immediately discontinue sale/use of the products and place all inventory in quarantine pending return to Medikmark. Distributors were instructed to sub-recall the kits from their customers. Any questions were directed to 1-847-596-7723.
Quantity9,100 kits
DistributionNationwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K920340SUTURE REMOVAL KIT
Medikmark, Inc., Apr 23, 1992