Clinical Technologies, Inc., 25 G Spinal Painpak, Reorder No.:4043, kit manufactured by Integra Spinal Specialties, San Antonio, Texas.
FDA Recall Z-0885-05 · Posted 2005-06-14
Recalling FirmSpinal Specialties, Inc
Recall StatusTerminated
Product CodeCAZ
Date Initiated2005-04-15
Date Terminated2005-11-02
Product Quantity100 kits
Reason for Recall
Becton Dickinson recalled the needles due to reports of leakage associated with an undersized Luer taper in the spinal needle hub.
Firm Action
The firm initiated the recall via letter on April 15, 2005.
Root Cause
Other
Distribution Pattern
VA, OH, TX, CA, IL, and FL
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.