Mahurkar QPlus Dual Lumen Catheter Kit with Curved Extension, 13.5 Fr/Ch x 19.5cm For hemodialysis, apheresis, and infusion. Reference: 8888-135192
FDA Recall Z-0233-04 · Posted 2003-12-17
Recalling FirmKendall Healthcare Products Co
Recall StatusTerminated
Product CodeMPB
Date Initiated2003-12-02
Date Terminated2012-05-15
Product Quantity45 units
Reason for Recall
Product is mislabeled to catheter length. Product labeled as a 13.5 Fr x 19.5 cm may contain a
13.5Fr x 16.0 cm
Firm Action
Kendall''s recall letters requesting product return will be hand delivered to customers by Kendall sales representatives on December 1, 2003.
Root Cause
Other
Distribution Pattern
IL, MA, OH, TN, TX, VA
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.