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FDA (Device enforcement)Recalled 2022-01-20class ii

Bard Peripheral Vascular Inc: LUMBAR PUNCTURE TRAY ADULT 18G X 3.5

Is my product affected?

LUMBAR PUNCTURE TRAY ADULT 18G X 3.5

  • UPC 10885403057021

Check against the official notice below — it lists the full affected range.

What happened

Bard Peripheral Vascular Inc. is recalling 8,630 Lumbar Puncture Tray Adult 18G X 3.5 devices distributed nationwide across the United States, Puerto Rico, Costa Rica, and Hong Kong. The recall was initiated due to manometer failure, which can result in leaking and mating issues with the device.

The affected devices carry catalog number 4303C and were manufactured with various lot numbers between March and September 2022. The source document does not specify a remedy or recommended course of action for affected consumers.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

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

Details from the source

Reason for recall: Due to lumbar puncture tray manometer failure mode of leaking and mating issues. 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: 8,630 devices Lot/code info: Catalog Number: 4303C Lot Numbers/UDI (GTIN, DI + PI): 0001411294 (01)10885403057021(17)220331(10)0001411294 0001414259 (01)10885403057021(17)220331(10)0001414259 0001414361 (01)10885403057021(17)220331(10)0001414361 0001415025 (01)10885403057021(17)220430(10)0001415025 0001417547 (01)10885403057021(17)220430(10)0001417547 0001422377 (01)10885403057021(17)220630(10)0001422377 0001425366 (01)10885403057021(17)220630(10)0001425366 0001426588 (01)10885403057021(17)220630(10)0001426588 0001428500 (01)10885403057021(17)220630(10)0001428500 0001431408 (01)10885403057021(17)220630(10)0001431408 0001433267 (01)10885403057021(17)220831(10)0001433267 0001433868 (01)10885403057021(17)220930(10)0001433868

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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