Facility

INTL. MEDSURG CONNECTION, INC.

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

Key facts

1recalls · worst Class II

5inspections · worst OAI

1warning letters

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

FDA Establishment Identifier (FEI)	3000210101
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	935 N Plum Grove Rd Ste F Schaumburg, IL, US 60173
Registration status	Active · expires 2026
Parent company	INTL. MEDSURG CONNECTION, INC. (owner-operator 9028111)

Activity by year

Recalls (1)
Inspections (5)
Warning letters (1)

Devices registered here (1)

Needle, Hypodermic, Single Lumen
Product code FMI (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5570

Recalls & enforcement

Class IITerminated2017-06-23
Insufficient documentation to support product sterility claims.

FDA inspections (5)

VAI2025-10-17
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
NAI2023-08-30
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
NAI2018-09-17
No Action Indicated · Compliance: Devices
OAI2017-11-22
Official Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
OAI2016-09-16
Official Action Indicated · Compliance: Devices; Postmarket Assurance: 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.

FDA warning letters (1)

Warning Letter2017-05-08
Warning Letter (opens in a new tab) · Schaumburg Illinois

Source: U.S. FDA Compliance Actions Dashboard (opens in a new tab) (device warning letters, 2016–present). Data as of 2026-10-06. Each link opens an FDA search for the letter; FDA can take several weeks to post a letter, so a very recent one may not appear yet.

All facilities operated by INTL. MEDSURG CONNECTION, 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. “INTL. MEDSURG CONNECTION, INC. (FEI 3000210101) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3000210101-intl-medsurg-connection-inc/

Not open yet

Alerts for INTL. MEDSURG CONNECTION, INC.

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.