Maquet PowerLED 700 — Class II medical device recall Z-1730-2014
Terminated recall by Maquet Medical Systems USA, reported 2014-06-18, distributed nationwide. Maquet has identified an issue with the Maquet PowerLED 700 (certain serial numbers). One or several plastic f
| Recall number | Z-1730-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Maquet Medical Systems USA, Wayne, NJ, United States |
| Recall initiated | 2014-04-16 |
| Classified | 2014-06-06 |
| Reported by FDA | 2014-06-18 |
| Terminated | 2016-04-06 |
| Distributed | Nationwide (US) |
| Quantity | 1,169 units |
| Reason classes | device malfunction |
| Serial numbers | 100, 105, 106, 108, 111, 118, 120, 12012, 121, 122, 159, 20010, 20011, 20013, 20014, 20015, 20016, 20017, 20018, 20019, 20020, 20021, 20022, 20023, 20024 and 395 more |
Product
Maquet PowerLED 700. Product Usage; To provide illumination to the surgical area or the patient.
Reason for recall
Maquet has identified an issue with the Maquet PowerLED 700 (certain serial numbers). One or several plastic fixation tabs can break, which can cause the ambient light module to partially detach.
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-1730-2014. 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.