—#138905

Product

UROLOGY PACK 4/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .

FDA product code: KNX — Collector, Urine, (And Accessories) For Indwelling Catheter
Device class: Class 2
Medical specialty: Gastroenterology, Urology
510(k) numbers: K962652
Affected lot / code info: Code:9001521 Lots: 141015699 exp. 11/30/15 141115980 exp. 12/31/15 150116560 exp. 2/28/16 150116560 exp. 2/28/16 150217271 exp. 2/28/16 150317613 exp. 4/30/16 150317616 exp. 4/30/16 150317615 exp. 4/30/16 150518646 exp. 5/31/16 150418301 exp. 5/31/16 150518647 exp. 5/31/16 150418302 exp. 5/31/16 150619387 exp. 6/30/16

Why it was recalled

Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.

Root cause (FDA determination)

Packaging

Action the firm took

Customed issued an "URGENT VOLUNTARY MEDICAL DEVICE RECALL" notification letter dated July 10, 2015 to all affected customers. The letter identified the product, problem, and actions to be taken by the customer.

Recalling firm

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

Distribution

Distribution pattern: Distributed Only in Puerto Rico.

Timeline

Recall initiated: 2015-07-10
Posted by FDA: 2015-09-03
Terminated: 2017-04-12
Status: —

Source: openFDA Device Recall endpoint. Recall record ID #138905. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.