FDA Device Intelligence
HomeCardinal Health 200, LLC › CARDINAL HEALTH

CARDINAL HEALTH

Cardinal Health 200, LLC · Model 26A2808H · UDI-DI 10197106914151

PWY Prescription
0
510(k) clearances
57
Adverse events
21
Recalls
15
Facilities

Description

SAFTY LUMB PNCT 22GX3,5 KIT

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 Lidocaine Ampules due to qu
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 been identified that ma
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 been identified that ma
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.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.