Erbe USA Inc: Unit, Cryosurgical, Accessories

Recalling firm
Erbe USA Inc
Product
Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use
Reason
Probes may rupture/burst during activation
Classification
Class II
Category
medical device recall
Country
United States
Agency
FDA-DEVICES
Recall date
2026-02-12
Status
Open, Classified
Areas affected
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
Distribution
US Nationwide distribution, including Puerto Rico.

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/7e4824b7-5ef5-4b8e-a104-a07617b29b69