BrightView X — Class II medical device recall Z-2010-2019
Terminated recall by Philips Medical Systems (Cleveland) Inc, reported 2019-07-31, distributed nationwide. An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion afte
| Recall number | Z-2010-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Medical Systems (Cleveland) Inc, Cleveland, OH, United States |
| Recall initiated | 2019-06-10 |
| Classified | 2019-07-22 |
| Reported by FDA | 2019-07-31 |
| Terminated | 2020-07-24 |
| Distributed | Nationwide (US) |
| Quantity | 117 |
| Serial numbers | 11000003, 11000004, 11000005, 11000006, 11000007, 11000008, 11000009, 11000010, 11000011, 11000012, 11000013, 11000014, 11000015, 11000016, 11000017, 11000018, 11000019, 11000020, 11000022, 11000023, 11000024, 11000025, 11000026, 11000027, 11000028 and 92 more |
| Model numbers | 882478 |
Product
BrightView X , Model Number 882478
Reason for recall
An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released.
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-2010-2019. 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.