Facility

SLEEPNET CORPORATION

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

Key facts

1recalls · worst Class I

4inspections · 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)	1222088
Establishment type	Manufacture Medical Device
Location	5 MERRILL INDUSTRIAL DRIVE Hampton, NH, US 03842
Registration status	Active · expires 2026
Parent company	SLEEPNET CORPORATION (owner-operator 9024494)

Activity by year

Recalls (1)
Inspections (4)

Devices registered here (1)

Ventilator, Non-Continuous (Respirator)
Product code BZD (opens in a new tab) · Class II · Anesthesiology · 21 CFR 868.5905

Recalls & enforcement

Class IOngoing2024-03-01
Update to contraindications and warning language due to CPAP masks containing magnets.

FDA inspections (4)

NAI2024-07-10
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
NAI2022-04-28
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
NAI2020-10-22
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
VAI2016-07-18
Voluntary Action Indicated · Compliance: 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 SLEEPNET CORPORATION

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. “SLEEPNET CORPORATION (FEI 1222088) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1222088-sleepnet-corporation/

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