# China NMPA Product Recall - Dental implant tools - dental drill extension

Source: https://www.keypedia.com/records/china_product_recall/dentsply-implants-manufacturing-gmbh/71a05f50-d72c-4034-8f24-d77d7a8c58c0
Source feed: China

> China NMPA product recall for Dental implant tools - dental drill extension by DENTSPLY Implants Manufacturing GmbH published May 14, 2019. Recall level: Level 3. Dentsply Sirona Dental Products (Shanghai) Co., Ltd. initiated a voluntary Class III recall of speci

---

## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Dentsply Sirona Dental Products (Shanghai) Co., Ltd. is voluntarily recalling dental implant tools.
- Company Name: DENTSPLY Implants Manufacturing GmbH
- Publication Date: 2019-05-14
- Product Name: Dental implant tools - dental drill extension
- Recall Level: Level 3
- Recall Reason: The manufacturing issue involves a problem with the product's clamping function.
- Discovering Company: Dentsply Sirona Dental Products (Shanghai) Co., Ltd.
- Manufacturing Company: DENTSPLY Implants Manufacturing GmbH
- Summary: Dentsply Sirona Dental Products (Shanghai) Co., Ltd. initiated a voluntary Class III recall of specific dental implant tools, specifically dental drill extenders, on May 14, 2019. This action was prompted by a manufacturing issue that compromised the clamping function of the affected products. The recall involves devices manufactured by DENTSPLY Implants Manufacturing GmbH, which were registered under Shanghai Food and Drug Administration Medical Device Registration Number 2019-108. This regulatory action is overseen by the National Medical Products Administration (NMPA). The company proactively reported this issue, providing detailed information regarding the models, specifications, and batch numbers of the impacted devices in a Medical Device Recall Event Report Form. This voluntary recall demonstrates Dentsply Sirona's commitment to product safety and compliance with NMPA's medical device regulations. By taking this measure, the company ensures that any devices failing to meet quality standards are removed from circulation, thereby safeguarding patient safety. The Class III classification signifies that the use of, or exposure to, a violative product is unlikely to cause adverse health consequences. This proactive step reinforces adherence to quality and safety standards within the medical device industry.

Company: https://www.keypedia.com/companies/dentsply-implants-manufacturing-gmbh/f438d2bb-484b-47fe-97f7-0e4a5e33cf5e