Philips Avent Smart Ear Thermometer — Class II medical device recall Z-0689-2018
Terminated recall by Philips Consumer Lifestyle, reported 2018-02-28. Device may provide inaccurate measurements.
| Recall number | Z-0689-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Consumer Lifestyle, Stamford, CT, United States |
| Recall initiated | 2018-02-02 |
| Classified | 2018-02-22 |
| Reported by FDA | 2018-02-28 |
| Terminated | 2019-03-29 |
| Quantity | 45,141 |
| Model numbers | DL8740, SCH740 |
Product
Philips Avent Smart Ear Thermometer (SCH740), Philips Ear Thermometer (DL8740)
Reason for recall
Device may provide inaccurate measurements.
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-0689-2018. 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.