Recall Z-0795-2022— 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 18G X 3.5. 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 18G X 3.5
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.