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MEDLINE

CENTURION MEDICAL PRODUCTS CORPORATION · Model DYNDH1527 · UDI-DI 10193489190823

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

Description

NEONATAL LUMBAR PUNCTURE

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.

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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.