FDA Device Intelligence
HomeMedicon eG. Chirurgiemechaniker-Genossenschaft › Medicon

Medicon

Medicon eG. Chirurgiemechaniker-Genossenschaft · Model 52.26.74 · UDI-DI 04046826065324

HDF Prescription
10
510(k) clearances
44
Adverse events
3
Recalls
227
Facilities

Description

Breisky vag retr 170x35mm

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.
2023-03-16Carefusion 2200 IncA portion of the two products were incorrectly marked (etched) and packaged resulting in a product mismatch. The labels and laser etchings were switched on the two products.
2019-07-01Centurion Medical Products CorporationPotential for sterile packaging to be compromised

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.