FDA Device Intelligence
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Lumbar Puncture Tray (Adult & Pediatric)

FDA product code PWY · Class 2 · General Hospital

164
Registered devices
57
Adverse events
21
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-05-21Medline Industries, LPThe kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocai
2024-04-08MEDLINE INDUSTRIES, LP - NorthfieldMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have bee
2024-04-08MEDLINE INDUSTRIES, LP - NorthfieldMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have bee
2022-01-20Bard Peripheral Vascular IncDue to lumbar puncture tray manometer failure mode of leaking and mating issues.
2022-01-20Bard Peripheral Vascular IncDue to lumbar puncture tray manometer failure mode of leaking and mating issues.
2022-01-20Bard Peripheral Vascular IncDue to lumbar puncture tray manometer failure mode of leaking and mating issues.
2022-01-20Bard Peripheral Vascular IncDue to lumbar puncture tray manometer failure mode of leaking and mating issues.
2022-01-20Bard Peripheral Vascular IncDue to lumbar puncture tray manometer failure mode of leaking and mating issues.
2022-01-20Bard Peripheral Vascular IncDue to lumbar puncture tray manometer failure mode of leaking and mating issues.
2022-01-20Bard Peripheral Vascular IncDue to lumbar puncture tray manometer failure mode of leaking and mating issues.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.