FETZER MEDICAL GMBH & CO.KG
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
- Inspections (1)
Devices registered here (1)
- Chisel, Middle-EarProduct code JYE (opens in a new tab) · Class I · Ear, Nose, Throat · 21 CFR 874.4420
Recalls & enforcement
- Class IITerminated2018-12-28The firm had a report of doctors being unable to pull the obstetric forceps apart.
FDA inspections (1)
- VAI2018-09-27Voluntary Action Indicated · Compliance: Devices · citations posted
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “FETZER MEDICAL GMBH & CO.KG (FEI 3007648354) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3007648354-fetzer-medical-gmbh-co-kg/
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