RegWardenFDA facility compliance records
Recall

Class II — Thayer Medical Corporation

Recalling firmTHAYER MEDICAL CORP.
Registered facilityTHAYER MEDICAL CORPORTATION (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonInternal 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.
ProductAirLife® MiniSpacer® MDI Dispenser Adapter. Dual-Spray MiniSpacer® Metered Dose Inhaler (MDI) Dispenser/Adapter with 15 mm connections. The 15 mm Dual Spray MiniSpacer® is a Metered Dose Inhaler (MDI) Dispenser. It is a non-sterile, single-use item, intended to dispense aerosolized medication into a breathing circuit or ancillary circuits. MINISPACER adapters are indicated for patients on a breathing circuit, for whom aerosol medication has been prescribed, in short and long term critical care environments. The 15 mm device is installed and operated by licensed healthcare practitioners in …
Quantity19340
DistributionWorldwide Distribution - USA including CA, KY and Europe.
Initiated2012-06-06
Classified2012-07-02
Terminated2013-01-15
Recall numberZ-1927-2012
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Thayer Medical Corporation (Z-1927-2012).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/62283/

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