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
- GCY — Apparatus, 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.