Flexible Cryoprobe recall
Flexible Cryoprobe (OD 2.4mm, L1.15mm) REF: 20402-411. For surgical use
Why was Flexible Cryoprobe recalled?
Probes may rupture/burst during activation
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI: 04050147021846/ Expanded Lots:WO472498 WO472499 WO472615 WO472616 WO473794 WO473795 WO474908 WO474909 WO474910 WO475357 WO475358 WO477030 WO477513 WO477514 WO478643 WO478646 WO478647 WO478648 WO478843 WO478844;Initial 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
- Product
- Flexible Cryoprobe (OD 2.4mm, L1.15mm) REF: 20402-411. For surgical use
- Recalling firm
- Erbe USA Inc
- Quantity
- 3603 units
- Distribution
- US Nationwide distribution, including Puerto Rico.
- Recall date
- April 1, 2026
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)