22G Nerve Block PainPak, Reorder No.:3269, kit manufactured by Integra Spinal Specialties, San Antonio, Texas.
FDA device recall Z-0886-05 · posted 2005-06-14 · Terminated
Recall details
- Recalling firm
- Spinal Specialties, Inc
- Reason for recall
- Becton Dickinson recalled the needles due to reports of leakage associated with an undersized Luer taper in the spinal needle hub.
- Action taken
- The firm initiated the recall via letter on April 15, 2005.
- Root cause
- Other
- Status
- Terminated
- Product code
- CAZ
- Quantity affected
- 542 kits
- Distribution
- VA, OH, TX, CA, IL, and FL
- Date initiated
- 2005-04-15
- Date posted
- 2005-06-14
- Date terminated
- 2005-11-02
- Location
- San Antonio, TX
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