FDA Device Intelligence
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Needle, Aspiration And Injection, Reusable

FDA product code GDM · Class 1 · General, Plastic Surgery

729
Registered devices
56
Adverse events
4
Recalls
48
510(k) clearances

Devices with this code

Recent recalls

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

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.