RegWardenFDA facility compliance records
Recall

Class II — Fetzer Medical GmbH & Co. KG

Recalling firmFetzer Medical GmbH & Co.KG
Registered facilityFETZER MEDICAL GMBH & CO.KG (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonThe firm had a report of doctors being unable to pull the obstetric forceps apart.
Product12002 / Boss Instruments Ltd. Wrigley Obstetric Forceps, 11" (28cm), Item No./Product Code 46-5004 Fetzer Medical Obstetrical Forceps is a hand-held instruments intended to assist the birth of a foetus during difficult vaginal births through grasping the foetal head in order to facilitate its passage through the birth canal. The instruments are only used for female population. The product is non-powder, non-liquid, non-tablet, capsule or other.
Quantity10 units
DistributionUS Distribution to states of: IL and VA.
Initiated2018-12-28
Classified2019-01-18
Terminated2020-09-17
Recall numberZ-0756-2019
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Fetzer Medical GmbH & Co. KG (Z-0756-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/81873/

Not open yet

Alerts for Fetzer Medical GmbH & Co.KG

Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.

Planned

Want a one-page facility brief?

A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.