Philips Allura CV20 Interventional Fluoroscopic X-ray System products… — Class II medical device recall Z-0725-2022
Ongoing recall by Philips North America Llc, reported 2022-03-16, distributed nationwide. Due to a leak in the detector cooling system, cooling liquid may leak outside the drip tray of the chiller. If
| Recall number | Z-0725-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America Llc, Cambridge, MA, United States |
| Recall initiated | 2021-11-24 |
| Classified | 2022-03-04 |
| Reported by FDA | 2022-03-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AT, BD, BR, CH, CL, CN, DE, DK, DO, ES, FR, GB, GR, ID, IL, IN, IR, IT, JP, KR, LK, MX, MY, NL, PH, SA, TH, TR, TW, ZA |
| Quantity | 1 units |
| Reason classes | packaging |
| Model numbers | 722031 |
Product
Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a Laird chiller without an extended drip tray: Model Number: 722031
Reason for recall
Due to a leak in the detector cooling system, cooling liquid may leak outside the drip tray of the chiller. If this occurs the liquid may drip onto electrical components in the R cabinet located in the technical room, which could lead to damage to the system and potentially cause thermal events such as a burning odor, smoke or fire.
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-0725-2022. 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.