LUMBAR PUNCTURE DRUG FREE TRAY 22G
Check against the official notice below — it lists the full affected range.
Bard Peripheral Vascular Inc. is recalling 2,880 Lumbar Puncture Drug Free Trays with catalog number 4306CWDF due to manometer failure modes involving leaking and mating issues. The affected devices were distributed nationwide across all U.S. states and territories, as well as internationally to Costa Rica and Hong Kong, with expiration dates of July 31, 2025.
The recall involves five specific lot numbers: 0001415023, 0001416353, 0001420159, 0001424771, and 0001437270. The source document does not specify a remedy or instructions for consumers who may have affected devices.
Written by software from the official notice below. Not reviewed by a lawyer.
Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
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: 2,880 devices Lot/code info: 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
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.