Every recall we track for ZOLL Medical Corporation — 13 in all — plus the complaints and injury reports the public filed about them.
ZOLL Powerheart G5 AED model G5S-80A may fail self-tests due to extreme temperatures or humidity. Affected units have serial numbers listed in the recall. Consumers should check if their device is affected and follow the official remedy steps.
ZOLL Powerheart G5 AEDs (models G5A-80C and G5A-80C-TSO) may fail self-tests if exposed to extreme temperatures or humidity. This recall affects specific units with serial numbers listed in the notice. No action is required for normal use, but users should check if their device is affected before use.
ZOLL Powerheart G5 AED models G5A-80A and G5A-80A-TSO may fail self-tests due to extreme temperatures or humidity. Affected units have serial numbers listed in the recall. Consumers should check their device for the specific model and serial number.
ZOLL recalls Powerheart G5 AED models G5A-00A to G5A-80A-TSO due to potential failure in self-tests from extreme temperatures or humidity. No action needed if device is in normal use conditions.
ZOLL recalls Powerheart G5 AED models G5S-00A-TSO through G5S-90A due to potential self-test failure from prolonged exposure to extreme temperatures or humidity. No remedy is specified in the recall notice.
ZOLL recalls Powerheart G5 AED models G5S-01C, G5S-02C, G5S-10C, and G5S-11C due to potential self-test failures from extreme temperatures or humidity. Affected units may not function properly during cardiac emergencies.
ZOLL recalls Powerheart G5 AED models G5A-01C to G5A-90C due to potential self-test failure from extreme temperatures or humidity. No remedy specified in official notice.
ZOLL recalls Powerheart G5 AED model G5S-80C due to potential failure in extreme temperatures or humidity. Affected units have serial numbers listed in the recall. No injuries reported; users should check if their device is affected and follow the recall instructions.
Zoll recalls Powerheart G5 AED models with protective film on front panel that may prevent shock button activation during cardiac arrest emergencies. Affected units include specific model numbers and serial ranges.
ZOLL Medical recalls MRI-compatible ventilator manuals that omit patient safety details. Update ensures safe MRI distance to prevent ventilator therapy delays.
ZOLL Medical Corporation recalls AED PRO devices that may fail to deliver energy to patients during cardiac arrest. Affected units have specific serial numbers and part numbers listed. Users should stop using and contact ZOLL for replacement.
