Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LUMBAR PUNCTURE DRUG FREE TRAY 22G Recalled by Bard Peripheral Vascular Inc Due to Due to lumbar puncture tray manometer failure mode...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Bard Peripheral Vascular Inc directly.
Affected Products
LUMBAR PUNCTURE DRUG FREE TRAY 22G
Quantity: 2,880 devices
Why Was This Recalled?
Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bard Peripheral Vascular Inc
Bard Peripheral Vascular Inc has 136 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report