Facility

THAYER MEDICAL CORPORTATION

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

Key facts

2recalls · 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)	2026894
Establishment type	Manufacture Medical Device
Location	4575 S PALO VERDE RD STE 337 TUCSON, AZ, US 85714
Registration status	Active · expires 2026
Parent company	THAYER MEDICAL CORP. (owner-operator 2026894)
Brand names	LITEAIRE® COLLAPSIBLE VALVED HOLDING CHAMBER

Activity by year

Recalls (2)
Inspections (1)

Devices registered here (1)

Holding Chambers, Direct Patient Interface
Product code NVP (opens in a new tab) · Class II · Anesthesiology · 21 CFR 868.5630

Recalls & enforcement

Class IITerminated2016-09-29
The insert and case label description of the device incorrectly reads Counter Incrementing Actuator with 22mm O.D./I.D. Connections.
Class IITerminated2012-06-06
Internal data identified a molding defect in the 15 mm O.D. / I.D. MiniSpacer meter dose inhaler (MDI) adapter that results in an incomplete fill of the aerosol dispensing pathway.

FDA inspections (1)

NAI2016-12-01
No Action Indicated · Compliance: Devices; Postmarket Assurance: 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 THAYER MEDICAL CORP.

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. “THAYER MEDICAL CORPORTATION (FEI 2026894) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2026894-thayer-medical-corportation/

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