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Terminated

22G Nerve Block PainPak, Reorder No.:3269, kit manufactured by Integra Spinal Specialties, San Antonio, Texas.

FDA Recall Z-0886-05 · Posted 2005-06-14

Recalling FirmSpinal Specialties, Inc
Recall StatusTerminated
Product CodeCAZ
Date Initiated2005-04-15
Date Terminated2005-11-02
Product Quantity542 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.

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