LUMBAR PUNCTURE TRAY ADULT 18G X 3.5
Reported: March 23, 2022 Initiated: January 20, 2022 #Z-0795-2022
Product Description
LUMBAR PUNCTURE TRAY ADULT 18G X 3.5
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
- 8,630 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? ▼
LUMBAR PUNCTURE TRAY ADULT 18G X 3.5. Recalled by Bard Peripheral Vascular Inc. Units affected: 8,630 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-0795-2022.
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