Cryoprobe Recall: Erbe USA Removes Flexible Cryoprobes
Recall Summary Erbe USA is recalling flexible Cryoprobes that may rupture when activated, potentially causing hearing loss, tinnitus, injury, or burns to users. The recall affects Cryoprobes distributed by the company for medical use. Healthcare facilities and practitioners who use these devices are included in this recall.
- Recalling firm
- Cryoprobe
- Reason
- Erbe Cryoprobes may rupture during activation, leading to potential hearing loss, tinnitus, injury, or burns.
- Category
- drug recall
- Country
- United States
- Agency
- FDA-MEDWATCH-RSS
- Recall date
- 2026-05-28
- Status
- Ongoing
Official recall notice from FDA-MEDWATCH-RSS
Recall details on Nibble Recalls: https://trynibble.app/recalls/0469e3a5-5619-49c4-a481-9c23464bd7c4