McKesson 33Recalls & reported problems
Mckesson Medical-Surgical Inc. · CRYOTHERAPY KIT, TRTMT · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20612479193974), received between Feb 23, 2026 and Feb 23, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Human-Device Interface Problem” (2 reports).
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
- Human-Device Interface Problem2
Patient problems
- Superficial (First Degree) Burn2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 23, 2026Human-Device Interface Problem
PLANTAR WART REMOVAL. CUSTOMER SAID THE INSERT STATED TO HOLD IT ON THE PLACE OF APPLICATION FOR 20 SECS. THEY BELIEVE THIS IS TOO LONG. PATIENT SUFFERED BURN LIKE INJURY TO TOE. MEDICAL TREATMENT WAS NECESSARY.
Patient problems: Superficial (First Degree) Burn
MAUDE report 24424080 ↗MalfunctionFeb 23, 2026Human-Device Interface Problem
PLANTAR WART REMOVAL ON FINGER. HELD THE DEVICE ON PLACE OF APPLICATION FOR 20 SECONDS. PATIENT SUFFERED BURN LIKE INJURY TO FINGER. MEDICAL TREATMENT WAS NECESSARY.
Patient problems: Superficial (First Degree) Burn
MAUDE report 24423789 ↗
Other Unit, Cryosurgical, Accessories devices
- IceFORCE® 2.1 CX 90° Cryoablation Needle FPRPR3602Boston Scientific Corporation · Unit, Cryosurgical, Accessories2 recalls4 deaths274 reports
- IceRod® 1.5 CX 90° Cryoablation Needle FPRPR3533Boston Scientific Corporation · Unit, Cryosurgical, Accessories1 recall168 reports
- IcePearl® 2.1 CX 90° Cryoablation Needle FPRPR3601Boston Scientific Corporation · Unit, Cryosurgical, Accessories2 recalls78 reports
- IceFORCE™ 2.1 CX L 90° Cryoablation Needle FPRPR3618Boston Scientific Corporation · Unit, Cryosurgical, Accessories2 recalls6 reports
- IceFORCE® 2.1 CX Cryoablation Needle FPRPR3604Boston Scientific Corporation · Unit, Cryosurgical, Accessories2 recalls3 reports
- IcePearl™ 2.1 CX L 90° Cryoablation Needle FPRPR3617Boston Scientific Corporation · Unit, Cryosurgical, Accessories2 recalls1 report
- Three IceFORCE ® 2.1 CX Prostate Cryoablation Kit Visual-ICE® System FPRPR3607Boston Scientific Corporation · Unit, Cryosurgical, Accessories2 recalls0 reports
- Three IcePearl® 2.1 CX Prostate Cryoablation KitVisual-ICE® System FPRPR3608Boston Scientific Corporation · Unit, Cryosurgical, Accessories2 recalls0 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page