Home › MibeTec GmbH › bite away
bite away
MibeTec GmbH · Model VI00545 · UDI-DI 04260624040295
1
510(k) clearances
6,882
Adverse events (12 deaths)
24
Recalls
277
Facilities
Description
The bite away® is a handheld device that allows the user to apply a therapeutic dose of heat directly to an insect sting or bite and is clinically proven to provide temporary relief of the resulting itching, pain and swelling. If the device is applied immediately after the sting or bite, the symptoms can usually be prevented completely. Even if the device is used slightly later, the symptoms can still subside sooner. bite away® works solely by concentrated heat and is thus completely free from chemicals (also suitable for pregnant women, allergy sufferers and children).
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-02-18 | Navajo Manufacturing Company | If heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by placing pad under the body, then t |
| 2024-02-08 | EYE COMFORT CARE LLC | Due to a change in the safety clips for the heated eye masks, the wires to the safety clips may detach as a result of tugging and pulling and may cause a short in the heating eleme |
| 2022-10-24 | Whele LLC DBA Perch | The products may have the potential to burn customers. Firm has received complaints of burns, mild shocks, and rashes/irritation. |
| 2022-10-24 | Whele LLC DBA Perch | The products may have the potential to burn customers. Firm has received complaints of burns, mild shocks, and rashes/irritation. |
| 2022-10-24 | Whele LLC DBA Perch | The products may have the potential to burn customers. Firm has received complaints of burns, mild shocks, and rashes/irritation. |
| 2016-09-15 | Battle Creek Equipment Co. | Products manufactured with the SPT cord have a known failure mode of sparking,causing smoke, fire and burns. |
| 2016-04-15 | 2k Innovations Inc. | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. |
| 2016-04-15 | 2k Innovations Inc. | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. |
| 2016-04-15 | 2k Innovations Inc. | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. |
| 2016-04-15 | 2k Innovations Inc. | During an FDA inspection it was found that the firm claims unapproved therapy and medical claims on product information and website. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.