—#129234

Product

FANFOLD DRAPE - CUSTOMED (1) DRAPE SHEET 42" X 57" SMS (1) WRAPPER 24" X 24" EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.

FDA product code: KKX — Drape, Surgical
Device class: Class 2
Medical specialty: General, Plastic Surgery
Affected lot / code info: Product code 900-633, 56 lots: 109020284 109040849 109051210 109071550 109092075 109102340 109112583 109122699 110010102 110010242 110020460 110030683 110030781 110041029 110051365 110071704 110082030 110092351 110102554 110102670 110122940 111010146 111020229 111030685 111040913 111051394 111051461 111061682 111061683 111071941 111071967 111082323 111092606 111102772 112041342 112052001 112062213 112062502 112083438 112093948 113036375 113036674 113036735 113047026 113057496 113068177 113078605 113089078 113099293 113109865 131110269 131210834 140211674 140412471 140412797 140513350

Why it was recalled

Customed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). This could result in an injury to the patient due to product contamination or loss of sterility condition.

Root cause (FDA determination)

Package design/selection

Action the firm took

Customed Inc. sent a Recall Notification letter dated June 3, 2014 via email and followed by letter to all affected customers. The letter identified the affected products, problem and actions to be taken. The letter informed customers if the affected products are in their inventory to: 1. Remove products from sale (quarantine them) and cease distribution. 2. Complete and return the enclosed acknowledgement form to Customed Inc .Recall Coordinator. Affected products should be returned to Customed Inc for credit. Customers with questions were instructed to contact Customed Inc. Recall Coordinator at 1-787-801-0100 Ext. 7540

Recalling firm

Firm: Customed, Inc Calle Igualdad Final # 7
Address: Fajardo, Puerto Rico 00738

Distribution

Distribution pattern: Worldwide Distribution - US (nationwide) in the state of Florida including Puerto Rico (USA); & USVI (St John) and the countries of Tortola, Trinidad, Dominican Republic, Costa Rica and Mexico.

Timeline

Recall initiated: 2014-05-20
Posted by FDA: 2014-08-29
Terminated: 2017-08-14
Status: —

Source: openFDA Device Recall endpoint. Recall record ID #129234. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.