BiPAP A30 Ventilator — Class I medical device recall Z-1814-2024
Ongoing recall by Philips Respironics, Inc., reported 2024-05-29, distributed nationwide. Potential for devices to experience interruption/loss of therapy during a Ventilator Inoperative alarm. This m
| Recall number | Z-1814-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Respironics, Inc., Murrysville, PA, United States |
| Recall initiated | 2024-03-26 |
| Classified | 2024-05-23 |
| Reported by FDA | 2024-05-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BE, CY, CZ, DE, DK, ES, FR, HU, IT, NL, PL, PT, RO, RS, SK, TR |
| UPC / GTIN / UDI-DI | 00100866312535, 00100867632243, 00100868101717, 00100868123405, 00101173411874, 00101173501025, 00101605387999, 00101605492518, 00102715708933, 00103081362590, 00103081477911, 00103081545252, 00103907230980, 00103908446328, 00103911780389, 00106383900125, 00108782579254, 00110817569772, 00112497461414, 00113841175568, 00115802309715, 00115810662598, 00119184875493, 00119592507726, 00120604935376 and 331 more |
| Serial numbers | 1589B, 2200AAD, 2226666D6A7, 5353DF, L20896099B9E2, L20896114F61B, L2143745010D0, L2143750217A6, L21437503062F, L218354134DA9, L21835429C89B, L218354411003, L21835487DC95, L2183549292E0, L22559558FFDB, L22559559EE52, L2255956059FB, L225595636B60, L225595641FDF, L272147639435, L272147682AE6, L272147693B6F, L292412627223, L2924127048E9, N09765363D900 and 475 more |
| Model numbers | 1111143, 1111144, 1111144L, 1111144M, 1111144V, 1111145, 1111147, 1111148, 1111149, 1111150, 1111154, 1111181, 1116155, BR1111143, CN1111143, R1111143, R1111150, R1111181 |
Product
BiPAP A30 Ventilator, Part Number 1111143 (US and OUS) OUS Only: Part Numbers 1111144 1111145 1111147 1111148 1111149 1111150 1111154 1111181 1116155 1111144L 1111144M 1111144V BR1111143 CN1111143 R1111143 R1111150 R1111181
Reason for recall
Potential for devices to experience interruption/loss of therapy during a Ventilator Inoperative alarm. This may lead to hypoventilation, mild to severe hypoxemia, hypercarbia, respiratory failure/insufficiency, or potentially death in the most vulnerable patients.
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-1814-2024. 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.