Accu-Temp® 8445000Recalls & reported problems
Beaver-Visitec International, Inc. · High Temperature Cautery · Class 2
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Jul 19, 2018Terminated
A small number of devices in this lot may have a melted cap and a hole formed through the packaging. The risk is potentially the product will no longer be sterile for use and may cause harm to a patient.
Z-3045-2018 · Root cause: Nonconforming Material/Component · FDA record ↗
Other Unit, cautery, thermal, battery-powered devices
- BVI OME6001UBeaver-Visitec International, Inc. · Unit, cautery, thermal, battery-powered1 recall0 reports
- Bovie AA01Aspen Surgical Products, Inc. · Unit, Cautery, Thermal, Battery-Powered23 reports
- Bovie AA05Aspen Surgical Products, Inc. · Unit, Cautery, Thermal, Battery-Powered10 reports
- Bovie AA21Aspen Surgical Products, Inc. · Unit, Cautery, Thermal, Battery-Powered4 reports
- Argent 231Mckesson Medical-Surgical Inc. · Unit, Cautery, Thermal, Battery-Powered3 reports
- Accu-Temp® 8442000Beaver-Visitec International, Inc. · Unit, cautery, thermal, battery-powered3 reports
- Argent 244Mckesson Medical-Surgical Inc. · Unit, Cautery, Thermal, Battery-Powered2 reports
- Bovie AA01XAspen Surgical Products, Inc. · Unit, Cautery, Thermal, Battery-Powered2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.