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Medicon eG. Chirurgiemechaniker-Genossenschaft · Model 01.51.02 · UDI-DI 04046826000561

GDX Prescription
10
510(k) clearances
127
Adverse events
6
Recalls
164
Facilities

Description

Dieffenbach scalpel 16cm fig 2

Recalls

DateFirmReason
2017-11-06Southmedic, Inc.Scalpels lot contains non-sterile products labeled as sterile.
2015-08-18Zien Medical Technologies, IncCracks were discovered in the PET tray of a small population of sterile product. These cracks create a risk of loss of sterile barrier for the product. Sampling and root cause anal
2013-02-07Myco Medical Supplies IncPouch labeling/printing errors and defective packaging resulting in possible compromised sterility.
2010-09-03Southmedic, Inc.Scalpels labeled as sterile have the potential to be unsealed and therefore not sterile.
2010-09-03Southmedic, Inc.Scalpels labeled as sterile have the potential to be unsealed and therefore not sterile.
2010-09-03Southmedic, Inc.Scalpels labeled as sterile have the potential to be unsealed and therefore not sterile.

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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.