Braun Thermoscan¿ PRO 6000 Ear Thermometer — Class II medical device recall Z-2339-2024
Ongoing recall by Baxter Healthcare Corporation, reported 2024-07-17, distributed in GU, PR. The Braun Thermoscan PRO 6000 ear thermometers may have been shipped with a compact disc (CD) containing an ou
| Recall number | Z-2339-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2024-06-13 |
| Classified | 2024-07-11 |
| Reported by FDA | 2024-07-17 |
| Distributed | GU, PR |
| Countries outside the US | AE, AF, AT, AU, BE, BH, BO, BS, CA, CH, CL, CO, CY, CZ, DE, DK, EC, EE, ES, FI, FR, GB, GR, GT, HK, HR, HU, IE, IL, IN, IQ, IS, IT, JO, KR, KW, MX, MY, NL, NO, NZ, OM, PA, PH, PL, PT, QA, SA, SE, SG, SI, TH, TR, TW, VN, ZA |
| Quantity | 265,647 units |
| UPC / GTIN / UDI-DI | 00732094309003, 00732094309027 |
Product
Braun Thermoscan¿ PRO 6000 Ear Thermometer
Reason for recall
The Braun Thermoscan PRO 6000 ear thermometers may have been shipped with a compact disc (CD) containing an outdated version of the Instructions for Use (IFU).
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-2339-2024. 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.