Facility

MICROMEDICS, INC.

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

Key facts

1recalls · worst Class II

1inspections · worst NAI

—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)	2183425
Establishment type	Manufacture Medical Device
Location	1270 Eagan Industrial Road Saint Paul, MN, US 55121
Registration status	Active · expires 2026
Parent company	Micromedics, Inc. (owner-operator 2183425)
Brand names	Duplospray MIS Applicator with Snap Lock; BAXTER DUPLOSPRAY MIS APPLICATOR

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (1)

Syringe, Piston
Product code FMF (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5860

Recalls & enforcement

Class IITerminated2016-10-20
The sterile packaging may contain small channels in the seal of the pouch, If the channels are present, the package integrity may be compromised which may affect sterility assurance.

FDA inspections (1)

NAI2017-05-09
No Action Indicated · Compliance: Devices

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.

All facilities operated by Micromedics, Inc.

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. “MICROMEDICS, INC. (FEI 2183425) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2183425-micromedics-inc/

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