Facility

MED MICHIGAN HOLDINGS LLC

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)	3017540705
Establishment type	Manufacture Medical Device
Location	1017 4th Ave Lake Odessa, MI, US 48849
Registration status	Active · expires 2026
Parent company	MED Michigan Holdings LLC (owner-operator 10078584)
Brand names	Perfusion Set, Y-Type; Perfusion Set, Recirculating; Multiple Perfusion Set; Perfusion Set, Straight; Multiple Perfusion Set with Vent; Perfusion Set, Y-Type with Vent

Activity by year

Recalls (1)

Devices registered here (1)

Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Product code DWF (opens in a new tab) · Class II · Cardiovascular · 21 CFR 870.4210

Recalls & enforcement

Class IIOngoing2024-11-19
Incomplete or partial pouch seals, which may result in a breach in the sterility.

All facilities operated by MED Michigan Holdings LLC

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. “MED MICHIGAN HOLDINGS LLC (FEI 3017540705) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3017540705-med-michigan-holdings-llc/

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