Covidien Healthcare International Trading (Shanghai) Co., Ltd. reported that due to the risk of overheating in the battery component of the video laryngoscope, which may cause harm to caregivers or patients, the manufacturer Covidien LLC has voluntarily recalled its produced Video Laryngoscope (Imported Medical Device Registration No. 20172227144), and McGRATH MAC Video Laryngoscope (Imported Medical Device Registration No. 20222080633). The recall is classified as a Level 1 recall. For detailed information regarding the models, specifications, and batches of the affected products, please refer to the "Medical Device Recall Event Report."

Attachment:Medical Device Recall Incident Report Form.pdf

August 13, 2023