Vapor-Clean — Class II medical device recall Z-1591-2023
Ongoing recall by Dynasthetics LLC, reported 2023-05-24. Due to a manufacturing issue that may result in filter leakage.
| Recall number | Z-1591-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Dynasthetics LLC, Salt Lake City, UT, United States |
| Recall initiated | 2022-05-09 |
| Classified | 2023-05-16 |
| Reported by FDA | 2023-05-24 |
| Countries outside the US | AU |
| Quantity | 28 filters |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 30858545007012 |
| Lot numbers | 0222P |
| Model numbers | 111AU |
Product
Vapor-Clean, Part Number 111AU The Vapor-Clean filter is intended to be used to remove unwanted anesthetic gases from the patient breathing circuit. The device uses two anesthetic vapor adsorbent canisters connected to an anesthesia delivery system to prevent unwanted anesthetic vapors emanating from within an anesthesia gas machine from reaching a patient.
Reason for recall
Due to a manufacturing issue that may result in filter leakage.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1591-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.