# China NMPA Product Recall - Ultrasonic High-Frequency Surgical Integrated System Ultrasonic Scalpel Head

Source: https://www.globalkeysolutions.net/records/china_product_recall/ethicon-endo-surgery-llc/5cef5524-55e7-4ebb-8f2a-4da199348ee1/
Source feed: China

> China NMPA product recall for Ultrasonic High-Frequency Surgical Integrated System Ultrasonic Scalpel Head by Ethicon Endo-Surgery, LLC published December 21, 2015. Recall level: . The National Medical Products Administration (NMPA) released a recall notice on December 21, 2015, c

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Synthes GmbH recalls ultrasonic scalpel tips for its high-frequency surgical integrated system.
- Company Name: Ethicon Endo-Surgery, LLC
- Publication Date: 2015-12-21
- Product Name: Ultrasonic High-Frequency Surgical Integrated System Ultrasonic Scalpel Head
- Recall Reason: In extreme cases, the interaction between the advanced hemostasis (green) button and the Tyvek packaging may damage the product's Tyvek packaging, thereby compromising the product's sterility barrier. Damage to the sterility barrier may lead to microbial infection in the patient.
- Discovering Company: Johnson & Johnson (Shanghai) Medical Devices Co., Ltd.
- Manufacturing Company: Ethicon Endo-Surgery, LLC
- Summary: The National Medical Products Administration (NMPA) released a recall notice on December 21, 2015, concerning ultrasonic scalpel tips for integrated high-frequency surgical systems. The recall was initiated globally by Ethicon Endo-Surgery, LLC, the manufacturer Synthes GmbH, and reported by Johnson & Johnson (Shanghai) Medical Devices Co., Ltd. on November 27, 2015. The core issue involves a compromised sterile barrier function: the interaction between the "Advanced Hemostasis" button and the Tyvek packaging could damage the packaging, potentially leading to a loss of sterility and subsequent microbial infection risk for patients. Although this is a global recall, Johnson & Johnson (Shanghai) Medical Devices Co., Ltd. confirmed that the affected product batches (models HARH23, HARH36, HARH45) were neither imported nor sold within China. Consequently, no direct product retrieval actions were required in the Chinese market. The NMPA's regulatory framework mandates that provincial food and drug administrations strengthen their supervision over such products. The recall aims to prevent potential patient risks associated with compromised sterility, even though no adverse event reports related to this specific issue have been received globally.

Company: https://www.globalkeysolutions.net/companies/ethicon-endo-surgery-llc/dfce5be3-6a9d-4239-8ba0-5d5283b81a02/