medical HIGH RISK Updated 2026-04-01

Erbe USA Inc recalls Flexible Cryoprobe (OD 2.4mm, L1.15mm) REF: 20402-411. For

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Recalled Product

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

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Hazard / Issue

Probes may rupture/burst during activation

Issued by

FDA

Distribution: Nationwide (United States)
Lot/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

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

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View official government recall

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