Bard Peripheral Vascular Inc: Medical Device Recall in 2022 - (Recall #: Z-0800-2022)

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:

SAFE-T PLUS ATRAUMATIC ADULT LP TRAY

Product Classification:

Class II

Date Initiated: January 20, 2022

Date Posted: March 23, 2022

Recall Number: Z-0800-2022

Event ID: 89553

Reason for Recall:

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

Status: Ongoing

Product Quantity: 3,240 devices

Code Information:

Catalog Number: 4306CWSP Lot Numbers/UDI (GTIN, DI + PI): 0001416832 (01)10885403229008(17)220430(10)0001416832 0001417843 (01)10885403229008(17)220430(10)0001417843 0001421009 (01)10885403229008(17)220531(10)0001421009 0001424764 (01)10885403229008(17)220630(10)0001424764 0001428872 (01)10885403229008(17)220630(10)0001428872 0001436145 (01)10885403229008(17)220930(10)0001436145

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