# China NMPA Product Recall - Arterial blood collection device

Source: https://www.globalkeysolutions.net/records/china_product_recall/smith-medical-devices-shanghai-co-ltd/131959c1-3f25-4f81-8236-6e6f23cbd3c5/
Source feed: China

> China NMPA product recall for Arterial blood collection device by Smith Medical Devices (Shanghai) Co., Ltd. published March 17, 2017. Recall level: Level II. BD Medical Devices (Shanghai) Co., Ltd. initiated a voluntary Level II recall of specific arterial b

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: BD Medical Devices (Shanghai) Co., Ltd. voluntarily recalls arterial blood collection devices
- Company Name: Smith Medical Devices (Shanghai) Co., Ltd.
- Publication Date: 2017-03-17
- Product Name: Arterial blood collection device
- Recall Level: Level II
- Recall Reason: The company discovered that if a "click" sound was heard before the protective cover locked on the product in question, the protective cover may not have been fully locked.
- Discovering Company: BD Medical Devices (Shanghai) Co., Ltd.
- Manufacturing Company: Smith Medical Devices (Shanghai) Co., Ltd.
- Summary: BD Medical Devices (Shanghai) Co., Ltd. initiated a voluntary Level II recall of specific arterial blood collection devices, as announced by the National Medical Products Administration (NMPA) on March 17, 2017. The recall stems from a manufacturing anomaly where the protective cover on affected products might not fully lock, even after a "click" sound is heard during operation. This issue could lead to the cover not being securely fastened, posing a potential safety concern during device use. The company's investigation revealed that the 'click' sound did not always signify a complete lock, prompting the recall to address this potential malfunction. Although the precise inspection dates are not specified in this recall notification, the action falls under the NMPA's regulatory oversight for medical device safety. As part of the corrective measures, BD Medical Devices (Shanghai) Co., Ltd. has advised users to visually inspect the device to confirm the protective cover is fully locked before use. Notably, the NMPA document states that products can continue to be used after this visual confirmation. Detailed information regarding the models, specifications, and batch numbers of the affected devices is provided in the accompanying "Medical Device Recall Event Report Form." This proactive measure aims to ensure patient safety and product integrity in accordance with NMPA guidelines.

Company: https://www.globalkeysolutions.net/companies/smith-medical-devices-shanghai-co-ltd/a4f694b0-5671-4759-922c-b6adb96ecceb/