Bard Peripheral Vascular Inc: Medical Device Recall in 2022 - (Recall #: Z-0799-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

LUMBAR PUNCTURE DRUG FREE TRAY 22G

Product Classification:

Class II

Date Initiated: January 20, 2022

Date Posted: March 23, 2022

Recall Number: Z-0799-2022

Event ID: 89553

Reason for Recall:

Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Status: Ongoing

Product Quantity: 2,880 devices

Code Information:

Catalog Number: 4306CWDF Lot Numbers/UDI (GTIN, DI + PI): 0001415023 (01)10885403231827(17)250731(10)0001415023 0001416353 (01)10885403231827(17)250731(10)0001416353 0001420159 (01)10885403231827(17)250731(10)0001420159 0001424771 (01)10885403231827(17)250731(10)0001424771 0001437270 (01)10885403231827(17)250731(10)0001437270

Distribution Pattern:

U.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 Kong.

Voluntary or Mandated:

Voluntary: Firm initiated