Facility

HUMAN MED AG

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3003587189
Establishment type	Manufacture Medical Device
Location	WILHELM-HENNEMANN-STR.9 SCHWERIN Mecklenburg-Western Pomerania, DE 19061
Registration status	Active · expires 2026
Parent company	Human Med AG (owner-operator 9043320)

Activity by year

Recalls (1)

Devices registered here (1)

Connector, Catheter
Product code GCD (opens in a new tab) · Class I · General, Plastic Surgery · 21 CFR 878.4200

Recalls & enforcement

Class IIOngoing2024-10-18
The cannula tubes do not comply with the specification. The water jet emerging from the nozzle of the nonconforming cannulas may emerge as a spot jet rather than a fan-shaped spray jet.

All facilities operated by Human Med AG

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. “HUMAN MED AG (FEI 3003587189) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003587189-human-med-ag/

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