Class I — UrgentReported 2026-04-01

Flexible Cryoprobe (OD 2.4mm, L1.15mm) REF: 20402-411. For surgical use

Recalled by Erbe USA Inc

Reason for Recall

Probes may rupture/burst during activation

Recall Number

Z-1568-2026

Classification

Class I

Status

Ongoing

Category

device

Initiated

2026-02-12

Reported

2026-04-01

Distribution

US Nationwide distribution, including Puerto Rico.

Code Info

UDI: 04050147021846/ Lots: WO461840 WO461846 WO462097 W2462284 WO463327 WO463328 WO463388 W2463594 WO464285 WO464286 WO465063 WO465064 W4465351 W2465601 W2465689 W2465749 W2465769 WO467873 WO467874 WO467875 WO468648 WO468649 WO469364 W2459861 W2459862 W2459863

Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.