Device recall
Z-2482-2021: Braun ThermoScan PRO 6000 Ear Thermometer-indicated for the intermittent…
FDA device recall · Class II · Welch Allyn Inc
Key facts
| Recall number (Z-number) | Z-2482-2021 |
|---|---|
| Recall event | 88481 |
| Product | Braun ThermoScan PRO 6000 Ear Thermometer-indicated for the intermittent measurement of human body temperature for patients having ages ranging from normal weight (full term) newborn to geriatric adults in a professional use environment. Model: 6000 |
| Product code | FLL |
| Recalling firm | Welch Allyn Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K152748 |
| FEI number | 1316463 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database