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Medicon

Medicon eG. Chirurgiemechaniker-Genossenschaft · Model 51.99.50 · UDI-DI 04046826063764

HFX Prescription
10
510(k) clearances
862
Adverse events (5 deaths)
14
Recalls
49
Facilities

Description

Mogen circumcision clamp

Recalls

DateFirmReason
2024-09-03MEDLINE INDUSTRIES, LP - NorthfieldProduct has been identified as having holes in the packaging.
2023-05-23MEDLINE INDUSTRIES, LP - NorthfieldThe kits incorrectly contain CirClamp subassembly 345CRSAK which results in the kits containing an incorrect bell and base size.
2023-03-02MEDLINE INDUSTRIES, LP - NorthfieldThe CirClamp subassembly found in the kit was the incorrect size.
2019-08-28Centurion Medical Products CorporationA mismatch between the angle of the hole in the base and the angle of the bell, which may cause the clamp to remove foreskin without the use of a scalpel.
2019-08-28Centurion Medical Products CorporationA mismatch between the angle of the hole in the base and the angle of the bell, which may cause the clamp to remove foreskin without the use of a scalpel.
2016-10-28Aesculap Implant Systems LLCAesculap has received complaints of excessive bleeding after use of Gomco Circumcision Clamps.
2014-09-08Instrumed International, Inc.The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet a
2014-09-08Instrumed International, Inc.The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet a
2014-01-16DeRoyal Industries IncThree lots of circumcision clamps were manufactured out of specification and as a result may not properly clamp at the surgical site completely.
2011-05-05Deroyal Industries, Inc. LafolletteThe firm distributed surgical kits which contained circumcision clamps that were subsequently recalled by Surgical Design.

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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.