# China NMPA Product Recall - Automated External Defibrillator

Source: https://www.globalkeysolutions.net/records/china_product_recall/physio-control-inc/d5002fcf-1f41-454c-a68b-2164d9e3bc87/
Source feed: China

> China NMPA product recall for Automated External Defibrillator by Physio-Control, Inc. published February 02, 2026. Recall level: Level 3 Recall. Physio-Control, Inc., a medical device manufacturer, has initiated a voluntary Class III recall of s

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Physio-Control, Inc. is voluntarily recalling its Automated External Defibrillator (AED).
- Company Name: Physio-Control, Inc.
- Publication Date: 2026-02-02
- Product Name: Automated External Defibrillator
- Recall Level: Level 3 Recall
- Recall Reason: Conductive adhesive separation exists in defibrillation electrodes.
- Discovering Company: Stryker (Beijing) Medical Devices Co., Ltd.
- Manufacturing Company: Physio-Control, Inc.
- Summary: Physio-Control, Inc., a medical device manufacturer, has initiated a voluntary Class III recall of specific batches of its Automated External Defibrillator. This recall, reported by Stryker (Beijing) Medical Devices Co., Ltd. to the National Medical Products Administration (NMPA) on February 2, 2026, addresses a critical product defect. The primary issue identified is the conductive adhesive separation of the defibrillator electrodes, which could compromise the device's functionality. This regulatory action is overseen by the NMPA in China, highlighting the framework for ensuring medical device safety and quality. The required action involves the voluntary recall of affected batches, with detailed information on specific models and specifications available in an accompanying Medical Device Recall Event Report Form. This measure underscores the company's commitment to compliance and patient safety within the NMPA's regulatory environment.

Company: https://www.globalkeysolutions.net/companies/physio-control-inc/c025f05e-3b2b-4081-a12e-0e310448bbe6/