medical HIGH RISK Updated 2026-04-01

Erbe USA Inc recalls Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For

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Recalled Product

Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. 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: 04050147021822/ Lots: WO459860 WO462187 WO462322 WO462390 WO462391 WO462392 WO462393 WO462396 WO462677 WO462678 WO463323 WO463324 WO463325 WO463326 WO463386 WO463387 WO464280 WO464281 WO464282 WO464283 WO464284 WO465059 WO465060 WO465061 WO465062 WO467876 WO467877 WO467878 WO467879 WO468225 WO468226 WO468227 WO468642 WO468643 WO468644 WO468645 WO468647 WO468671 WO468672 WO468673 WO468674 WO469361 WO469362 WO469363 W2459858 W2459958 W2462283 W2463593 W2465596 W2465623 W2465693 W2465768 W2468859 W2470050 W2470051 W2470052 W4465597

✅ 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?

Search Amazon for Flexible Cryoprobe (OD 1.7mm, →

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View official government recall

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