FDA Recall
Terminated
Mahurkar QPlus Dual Lumen Catheter Insertion Tray with Curved Extension, 13.5 Fr/Ch x 19.5cm For hemodialysis, apheresis, and infusion Reference: 8888-135195
Recall: Z-0234-04
·
Initiated December 2, 2003
Recall
- Recall Number
- Z-0234-04
- Event Number
- 27842
- Firm
- Kendall Healthcare Products Co
- FEI Number
- 1282497
- Product Code
- MPB
- Status
- Terminated
- Root Cause
- Other
- Initiated
- December 2, 2003
- Posted
- December 17, 2003
- Terminated
- May 15, 2012
- Address
- 15 Hampshire St, Mansfield, MA, 02048-1113
Description
Mahurkar QPlus Dual Lumen Catheter Insertion Tray with Curved Extension, 13.5 Fr/Ch x 19.5cm For hemodialysis, apheresis, and infusion Reference: 8888-135195
Reason
Product is mislabeled to catheter length. Product labeled as a 13.5 Fr x 19.5 cm may contain a 13.5 Fr x 16.0 cm
Action
Kendall''s recall letters requesting product return will be hand delivered to customers by Kendall sales representatives on December 1, 2003.
Distribution
IL, MA, OH, TN, TX, VA
Quantity
10