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ASPIRATION NEEDLE

OLYMPUS MEDICAL SYSTEMS CORP. · Model NA-2C-1 · UDI-DI 04953170035302

GDM Prescription

510(k) clearances

Adverse events (3 deaths)

Recalls

113

Facilities

Description

This model includes one of sheath section and six of needle sections. The sheath section is reusable and requires autoclave sterilization prior to use. The needle section is single-use and packaged as sterile. Please refer to the instruction manual for details.

Recalls

Date	Firm	Reason
2025-06-27	Spiggle & Theis Mt Gmbh	Affected product show elevated cytotoxicity values. Use of affected injection needles may present a risk of intolerance reaction or allergic reaction.
2015-01-08	Teleflex Medical	Packaging error in which customers who ordered product code 140880 (Verres cannula for use with a separately available needle tip) were incorrectly provided with product code 14087
2009-09-01	Medical Device Technologies, Inc.	Medical Device Technologies doing business as Angiotech has conducted a recall on Angiotech Breast Localization Needles, Soft Tissue Biopsy Needles, Vascular Access Needles, Bone B
2009-04-06	Remington Medical Inc.	Incorrect needle (Franseen Needle, FNM-1806) was packaged as a Chiba Needle Marked.

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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.