Facility

DALE MEDICAL PRODUCTS, INC.

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

Key facts

1recalls · worst Class II

1inspections · worst VAI

—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)	1214422
Establishment type	Manufacture Medical Device
Location	3 State Pier Rd New London, CT, US 06320
Registration status	Active · expires 2026
Parent company	DALE MEDICAL PRODUCTS, INC. (owner-operator 1214422)
Brand names	Dale ACE CONNECTOR WITH ENFit CONNECTION SYSTEM; Dale ACE CONNECTOR

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (1)

Tubes, Gastrointestinal (And Accessories)
Product code KNT (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.5980

Recalls & enforcement

Class IITerminated2017-03-24
ET Tube Holders contain an adhesive faceplate that may lose its adhesive properties and will not adhere to the patient's face.

FDA inspections (1)

VAI2022-03-29
Voluntary 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.

All facilities operated by DALE MEDICAL PRODUCTS, 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. “DALE MEDICAL PRODUCTS, INC. (FEI 1214422) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1214422-dale-medical-products-inc/

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