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UNOLOK

HINDUSTAN SYRINGES AND MEDICAL DEVICES LIMITED · Model 3ml (22G x 1 1/2'') · UDI-DI 08903347051891

FMF Prescription

510(k) clearances

53,081

Adverse events (66 deaths)

305

Recalls

548

Facilities

Description

UNOLOK Single Use Hypodermic Syringe Luer Lock , 3ml with 22G x 1 1/2'' (0.70 X 38mm) Needle, Blister Packed

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.