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Update on Erbe USA Flexible Cryoprobes Recall
The FDA has updated the Cryoprobe Recall: Erbe USA Removes Flexible Cryoprobes communication with additional affected lot numbers recently reported by the firm.
On May 4, Erbe published a press release containing additional affected lot numbers of the recalled device. The recommendations for what to do with the recalled devices have not changed.
This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it without correction.
Questions?
Customers in the U.S. with adverse reactions, quality problems, or questions about this recall should contact Erbe USA at 770-955-4400.
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