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Recall

Class I — Draeger, Inc.

Recalling firmDraeger, Inc.
Registered facilityDRAEGER, INC. (the firm's only registered facility)
ClassificationClass I
StatusOngoing
ReasonReports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
ProductHME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter.
Quantity1,019,782 units
DistributionWorldwide - US Nationwide distribution including in the states of AK, AZ, CA, CO, CT, FL, ID, IL, IN, KAS, LA, MA, ME, MI, MN, MO, NC, NE, NM, NV, NY, OH, PA, SD, TN, TX, UT, WA, WI, WY and the countries of Angola, Argentina, Australia, Austria, Belarus, Belgium, Bolivia, Bosnia-Herz., Brazil, Bulgaria, Burkina-Faso, Canada, Chile, China, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Dominic…
Initiated2025-06-16
Classified2025-07-31
Recall numberZ-2160-2025
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 I recall — Draeger, Inc. (Z-2160-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/97026/

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