FDA Device recall Z-2339-2024
Braun Thermoscan¿ PRO 6000 Ear Thermometer
- FDA Device
- Class II
- ongoing
- Published 2024-07-17
On 2024-07-17 the FDA classified a Class II recall of Braun Thermoscan¿ PRO 6000 Ear Thermometer by Baxter Healthcare, citing the Braun Thermoscan PRO 6000 ear thermometers may have been shipped with a compact disc (CD) containing an outdated version of the Instructions for Use (IFU).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2339-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-06-13 |
| Published | 2024-07-17 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Baxter Healthcare |
| Distribution | PR |
Product
Braun Thermoscan¿ PRO 6000 Ear Thermometer
Reason
The Braun Thermoscan PRO 6000 ear thermometers may have been shipped with a compact disc (CD) containing an outdated version of the Instructions for Use (IFU).
Identifiers
| code_info | UDI: 00732094309003 (product code 06000-200) and 00732094309027 (product code 06000-300); All serial numbers. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2339-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.