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Hermann Medizintechnik GmbH

Hermann Medizintechnik GmbH · Model H122-40408 · UDI-DI 04059453047380

GDM
10
510(k) clearances
56
Adverse events (3 deaths)
4
Recalls
113
Facilities

Description

REDON guide needle, Char.8, strongly curved lanceolate tip, Step Formation

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 with product code 14087
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 Access Needles, Bone B
2009-04-06Remington 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.