FDA Enforcement Class II Ongoing

ATRAUMATIC ADULT LUMBAR PUNCTURE TRAY

Recall: Z-0798-2022 · Reported March 23, 2022

Enforcement

Recall Number
Z-0798-2022
Event ID
89553
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Bard Peripheral Vascular Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
March 23, 2022
Initiation Date
January 20, 2022
Classification Date
March 16, 2022
Address
1625 W 3rd St Bldg 1, N/A, Tempe, AZ, 85281-2438, United States

Description

ATRAUMATIC ADULT LUMBAR PUNCTURE TRAY

Reason

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

Code Info

Catalog Number: 4306CW Lot Numbers/UDI (GTIN, DI + PI): 0001415028 (01)10885403228995(17)220430(10)0001415028 0001417842 (01)10885403228995(17)220430(10)0001417842 0001424355 (01)10885403228995(17)220630(10)0001424355 0001431413 (01)10885403228995(17)220630(10)0001431413 0001436376 (01)10885403228995(17)220930(10)0001436376

Distribution

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.

Quantity

2,880 devices