Verruca-Freeze VFC65Recalls & reported problems
CryoSurgery, Inc. · Verruca-Freeze 175ml Replacement Canister · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00865715000307), received between Aug 17, 2026 and Aug 17, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Off-Label Use” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Off-Label Use1
Patient problems
- Partial thickness (Second Degree) Burn1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 17, 2026Off-Label Use
On (b)(6) 2026, a licensed healthcare professional used a Verruca-Freeze cryosurgical system (lot VF2531502) to treat a large wart on the finger of a 14-year-old patient at a pediatric clinic. The practitioner selected a 9mm CryoCone applicator, pressed it to create a seal, and sprayed cryogen against the inside of the CryoCone. Cryogen leaked outside the CryoCone onto the patient's finger and through a towel onto the patient's thigh. Both areas became pink and were rinsed. The thigh became slightly raised shortly after. A thin layer of petroleum jelly was applied to both areas. By the following day, the patient developed large blisters on the finger requiring care at a burn hospital. The patient was diagnosed with a partial thickness burn on the finger requiring debridement and is receiving ongoing burn hospital follow-up. A first degree burn on the thigh is healing without complication.
Patient problems: Partial thickness (Second Degree) Burn
MAUDE report 50279546 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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