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Metier

Jiangsu Caina Medical Co.,Ltd · Model 1ml 25G*5/8" · UDI-DI 06971564467261

FMF MEG Prescription

510(k) clearances

53,081

Adverse events (66 deaths)

305

Recalls

544

Facilities

Description

The Safety Syringe with permanently attached needle is intended for use by health care professionals for general purpose aspiration of fluid from vials, ampoules and liquid injection below the surface of the skin. The Safety sheath of Syringe is designed to aid in the prevention of needle stick injuries and reduce the potential or syringe reuse.

Recalls

Date	Firm	Reason
2026-04-28	Mentor Texas LP	A single lot of expired syringes were distributed due to a distribution system control failure.
2026-04-21	ARROW INTERNATIONAL, LLC	Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo
2026-02-27	Cardinal Health 200, LLC	The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the syringes contained within the packages
2026-01-27	Becton Dickinson & Company	During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
2025-05-23	Integra LifeSciences Corp. (NeuroSciences)	Lack of sterility assurance.
2025-05-22	Integra LifeSciences Corp. (NeuroSciences)	Devices contain potentially out-of-specification levels of endotoxins and lack of sterility assurance.
2025-05-22	Integra LifeSciences Corp. (NeuroSciences)	Devices contain potentially out-of-specification levels of endotoxins and lack of sterility assurance.
2025-05-22	Integra LifeSciences Corp. (NeuroSciences)	Devices contain potentially out-of-specification levels of endotoxins and lack of sterility assurance.
2025-05-12	BD SWITZERLAND SARL	Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at the interface between the closed male luer component and the
2025-05-12	BD SWITZERLAND SARL	Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at the interface between the closed male luer component and the

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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.