Erbe
3 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Erbe and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-04-01FDA-DeviceClass IStop using Erbe USA Flexible Cryoprobe
Erbe USA Inc is recalling specific lots of Flexible Cryoprobe devices used in surgery because the probes may rupture or burst when activated. This defect could affect patient safety during the procedure. No injuries have been reported to date.
- 2026-04-01FDA-DeviceClass IStop using Erbe USA Flexible Cryoprobe devices
Erbe USA Inc. is recalling certain Flexible Cryoprobe surgical devices (model OD 1.7mm, L1.15mm, REF: 20402-410) because the probes may rupture or burst when activated during surgery. This defect could cause injury to patients or surgical staff. No injuries have been reported so far.
- 2026-04-01FDA-DeviceClass IStop using Erbe USA cryoprobes immediately
Erbe USA has recalled certain flexible cryoprobes used in surgery because they may rupture or burst when activated. The defect could cause unexpected device failure during a procedure. No injuries have been reported, but the risk requires immediate action.
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