Oxylog 3000 Plus emergency and transport ventilator — Class I medical device recall Z-2018-2023
Ongoing recall by Draeger Medical, Inc., reported 2023-07-19, distributed nationwide. Draeger has become aware of instances where the device stopped working when in use when transitioning from bat
| Recall number | Z-2018-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Draeger Medical, Inc., Telford, PA, United States |
| Recall initiated | 2023-06-12 |
| Classified | 2023-07-07 |
| Reported by FDA | 2023-07-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | AF, AR, AT, AU, BB, BE, BG, BH, BO, CA, CH, CL, CN, CR, CZ, DE, DK, DO, DZ, EC, EE, EG, ES, FI, FR, GB, GH, GR, HK, HN, HR, HU, ID, IE, IL, IN, IQ, IR, IT, JO, JP, KE, KR, KW, KY, LB, LK, LT, LV, MA, MT, MX, MY, NG, NL, NO, NP, NZ, OM, PA, PE, PK, PL, PT, PY, QA, RO, RS, SA, SE, SG, SI, SK, SV, TH, TN, TR, TT, TW, UA, UY, VN, ZA |
| Quantity | 300 units |
| UPC / GTIN / UDI-DI | 04048675398295 |
| Model numbers | 5704811, 5704813 |
Product
Oxylog 3000 Plus emergency and transport ventilator
Reason for recall
Draeger has become aware of instances where the device stopped working when in use when transitioning from battery to AC operation.
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-2018-2023. 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.