ClearanceBrief
Recall Z-0799-2022 ยท PWY Lumbar Puncture Tray (Adult & Pediatric)

Bard Peripheral Vascular Inc

LUMBAR PUNCTURE DRUG FREE TRAY 22G

DateJan 20, 2022
StatusOpen, Classified
ReasonDue to lumbar puncture tray manometer failure mode of leaking and mating issues.
Root causeProcess control
ActionBetween 01/28 and 02/01/2022, the firm sent an "URGENT MEDICAL DEVICE CORRECTION" Letter via email and FedEx 2-day mailings to customers informing them that between 07/02 to 12/15/2021 the firm received 59 customer complaints for lumbar puncture tray manometers with reported failure modes of leaking and mating issues. Customers are asked to take the following actions: 1. Check all inventory locations within their institution for the product listed in Table A and immediately destroy all affected product remaining in their possession. The product should have the sterile barrier broken and destr
Quantity2,880 devices
DistributionU.S. Nationwide Distribution: AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, Puerto Rico, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY. O.U.S. (foreign) including states: Costa Rica and Hong K
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.