Recalls / —
—#138987
Product
CENTRAL LINE FULL BODY DRAPE CUSTOMED 28/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
- KKX — Drape, Surgical
- Device class
- Class 2
- Medical specialty
- General, Plastic Surgery
- Affected lot / code info
- Code:9002262 Lots: 150217392 exp. 3/31/16 150116999 exp. 2/28/16 150518693 exp. 6/30/16 150619400 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 #138987. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.