FDA Device Recalls

Recalls /

#34453

Product

Jackson-Pratt Hemaduct, 15 Fr round, full duct silicone wound drain; a sterile, single use only, Rx device, individually packaged, 10 drains per box, 8 boxes per case; catalog #JP-HUR880; Allegiance Healthcare Corporation, McGaw Park, IL 60085 USA

FDA product code
GCYApparatus, Suction, Single Patient Use, Portable, Nonpowered
Device class
Class 1
Medical specialty
General, Plastic Surgery
Affected lot / code info
catalog #JP-HUR880, lot 1040909

Why it was recalled

The products labeled as sterile are not sterile.

Root cause (FDA determination)

Other

Action the firm took

The accounts were telephoned on 7/28/04 and sent follow-up letters on the same date. They were informed that affected lots of products were not sterile, and were requested to inspect their inventory and segregate the product for return to Cardinal Health. The accounts were instructed to call 800-635-6021 for product return and instructions on how to obtain credit and replacement product.

Recalling firm

Firm
Cardinal Health
Address
1430 Waukegan Rd, McGaw Park, Illinois 60085

Distribution

Distribution pattern
Florida, Arizona, New Jersey and Canada

Timeline

Recall initiated
2004-07-28
Posted by FDA
2004-08-25
Terminated
2005-02-10
Status

Source: openFDA Device Recall endpoint. Recall record ID #34453. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.