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Recall

Class II — Atrium Medical Corporation

Recalling firmATRIUM MEDICAL CORPORATION
Registered facilityAtrium Medical Corporation (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonThe Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the Express Mini 500 Dry Seal Chest Drains do not provide sufficient precaution against draining the device for continued use. Additionally, the IFUs do not provide sufficient precaution or warning against the use of the device outside the healthcare setting.
ProductExpress Mini 500 Dry Seal Chest Drain, Part Number 16400
Quantity8184 cases of 6
DistributionWorldwide distribution - US Nationwide and the countries of United Arab Emirates, Austria, Australia, Belgium, Brazil, Canada, Switzerland, Colombia, Czech Republic, Germany, Ecuador, Estonia, Spain, Finland, France, United Kingdom, Hong Kong, Indonesia, Ireland, Israel, Iceland, Italy, Jordan, South Korea, Kuwait, Luxembourg, Mexico, Malaysia, Netherlands, Norway, New Zealand, Peru, Philippines, …
Initiated2023-03-01
Classified2023-03-30
Recall numberZ-1303-2023
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 — Atrium Medical Corporation (Z-1303-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91718/

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