# China NMPA Product Recall - Bone screws

Source: https://www.globalkeysolutions.net/records/china_product_recall/synthes-gmbh/0aecf1d4-94ce-461f-8887-e2b942dfb5ce/
Source feed: China

> China NMPA product recall for Bone screws by Synthes GmbH published July 06, 2016. Recall level: Level II. Johnson & Johnson (Shanghai) Medical Devices Co., Ltd., in collaboration with manufacturer Synthes G

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Johnson & Johnson (Shanghai) Medical Devices Co., Ltd. voluntarily recalls bone screws.
- Company Name: Synthes GmbH
- Publication Date: 2016-07-06
- Product Name: Bone screws
- Recall Level: Level II
- Recall Reason: The manufacturer discovered that two batches of 20mm long 4.5mm cortical bone screws may contain 22mm long 4.5mm cortical bone screws, which could lead to surgical delays, damage to surrounding structures, or soft tissue irritation.
- Discovering Company: Johnson & Johnson (Shanghai) Medical Devices Co., Ltd.
- Manufacturing Company: Synthes GmbH
- Summary: Johnson & Johnson (Shanghai) Medical Devices Co., Ltd., in collaboration with manufacturer Synthes GmbH, initiated a voluntary Class II recall of specific bone screws, as reported by the National Medical Products Administration (NMPA) on July 6, 2016. The recall, detailed in a report dated May 11, 2016, addresses a critical product discrepancy: two batches of 20mm long 4.5mm cortical bone screws (Model 414.820, batch numbers including 2610310 and 3485895) were found to contain incorrectly sized 22mm long screws. This mixing of incorrect lengths presents potential risks, including prolonged surgical procedures as surgeons might need to identify and replace mispackaged screws. More critically, an improperly long screw, if inserted, could lead to adverse patient outcomes such as damage to surrounding structures, including articular surfaces, or cause soft tissue irritation if the issue goes undetected during surgery. While the recall applies globally, 27 affected items were imported into China, with no related complaints or adverse events reported in China at the time of the recall. Under the NMPA's oversight, Johnson & Johnson's required actions include notifying all affected customers to immediately cease using the identified product batches. Furthermore, all returned affected products are slated for local destruction to prevent any further use. This proactive recall underscores the company's commitment to patient safety and adherence to regulatory standards for medical devices.

Company: https://www.globalkeysolutions.net/companies/synthes-gmbh/77a06946-ba7a-4bf2-916a-600eabfb0ce7/