Spinal Specialties, Inc Clinical Technologies, Inc., 25 G Spinal Painpak, Reorder No.:4043, kit manufactured by Integra Spinal Specialties, San Antonio, Texas. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Clinical Technologies, Inc., 25 G Spinal Painpak, Reorder No.:4043, kit manufactured by Integra Spinal Specialties, San Antonio, Texas.
Brand
Spinal Specialties, Inc
Lot Codes / Batch Numbers
Lot number 1004328
Products Sold
Lot number 1004328
Spinal Specialties, Inc is recalling Clinical Technologies, Inc., 25 G Spinal Painpak, Reorder No.:4043, kit manufactured by Integra Spin due to Becton Dickinson recalled the needles due to reports of leakage associated with an undersized Luer taper in the spinal needle hub.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Becton Dickinson recalled the needles due to reports of leakage associated with an undersized Luer taper in the spinal needle hub.
Recommended Action
Per FDA guidance
The firm initiated the recall via letter on April 15, 2005.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, FL, IL, OH, TX, VA
Page updated: Jan 10, 2026