# China NMPA Product Recall - Burs disposable drill bits

Source: https://www.globalkeysolutions.net/records/china_product_recall/medtronic-xomed-inc/8ac15148-688e-44d5-a985-525aaa9fddb2/
Source feed: China

> China NMPA product recall for Burs disposable drill bits by Medtronic Xomed, Inc. published August 06, 2019. Recall level: Level 3 Recall. Medtronic Xomed, Inc., in collaboration with Medtronic (Shanghai) Management Co., Ltd., has initiate

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Medtronic Xomed, Inc. is proactively recalling its single-use drill bits, Burs.
- Company Name: Medtronic Xomed, Inc.
- Publication Date: 2019-08-06
- Product Name: Burs disposable drill bits
- Recall Level: Level 3 Recall
- Recall Reason: Issues where the diameter of some batches of products does not match the outer packaging label
- Discovering Company: Medtronic (Shanghai) Management Co., Ltd.
- Manufacturing Company: Medtronic Xomed, Inc.
- Summary: Medtronic Xomed, Inc., in collaboration with Medtronic (Shanghai) Management Co., Ltd., has initiated a voluntary Class III recall for its single-use drill bits Burs. This recall, announced by the National Medical Products Administration (NMPA) on August 6, 2019 (Index No. JGXX-2019-10501), addresses a critical discrepancy. The core issue involves certain product batches where the actual diameter of the drill bits did not align with the diameter printed on their outer packaging labels. This labeling inaccuracy mandates a recall to maintain product integrity and ensure patient safety. While specific inspection dates are not provided within this recall announcement, the company's voluntary action aligns with regulatory expectations for addressing product non-conformities.

The regulatory oversight for this recall falls under the NMPA, which is responsible for medical device safety and compliance in China. A Class III recall designation typically indicates that product use is unlikely to cause adverse health consequences but still represents a breach of regulatory requirements. The main required action for Medtronic is the thorough voluntary recall of all identified affected single-use drill bits Burs. Comprehensive details, including specific models, specifications, and batch numbers of the implicated products, are provided in the accompanying "Medical Device Recall Event Report Form." This ensures accurate identification and removal of non-compliant products from circulation, safeguarding against potential misuse.

Company: https://www.globalkeysolutions.net/companies/medtronic-xomed-inc/6ab04f9c-4587-45b0-ab74-0dfb3aa38e32/