Recall Z-0796-2022— Bard Peripheral Vascular Inc
Class II · Ongoing
Class II FDA medical device recall by Bard Peripheral Vascular Inc, initiated 2022-01-20. FDA's recall record names no specific 510(k) clearance for this event. Product: LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL. Reason: Due to lumbar puncture tray manometer failure mode of leaking and mating issues..
- Recalling firm
- Bard Peripheral Vascular Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-01-20
- Firm location
- Tempe, AZ, United States
Product description
LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL
Reason for recall
Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Data sourced from openFDA. This site is unofficial and independent of the FDA.