ADULT LUMBAR PUNCTURE DRUG FREE TRAY 20G
Reported: March 23, 2022 Initiated: January 20, 2022 #Z-0793-2022
Product Description
ADULT LUMBAR PUNCTURE DRUG FREE TRAY 20G
Reason for Recall
Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Details
- Recalling Firm
- Bard Peripheral Vascular Inc
- Units Affected
- 1260 devices
- 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.
- Location
- Tempe, AZ
Frequently Asked Questions
What product was recalled? ▼
ADULT LUMBAR PUNCTURE DRUG FREE TRAY 20G. Recalled by Bard Peripheral Vascular Inc. Units affected: 1260 devices.
Why was this product recalled? ▼
Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 23, 2022. Severity: Moderate. Recall number: Z-0793-2022.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11