# China NMPA Product Recall - Metal intramedullary nail surgical instruments

Source: https://www.globalkeysolutions.net/records/china_product_recall/zimmer-medical-shanghai-international-trading-co-ltd/492c3381-293f-429e-9d47-3d1927a6bce3/
Source feed: China

> China NMPA product recall for Metal intramedullary nail surgical instruments by Zimmer Medical (Shanghai) International Trading Co., Ltd. published July 14, 2017. Recall level: Level 2. Zimmer Medical (Shanghai) International Trading Co., Ltd. initiated a voluntary Class II recall of i

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Zimmer Medical (Shanghai) International Trading Co., Ltd. voluntarily recalls surgical instruments for intramedullary nailing.
- Company Name: Zimmer Medical (Shanghai) International Trading Co., Ltd.
- Publication Date: 2017-07-14
- Product Name: Metal intramedullary nail surgical instruments
- Recall Level: Level 2
- Recall Reason: The raw materials used in the product may be abnormal, which could increase the risk of product breakage.
- Discovering Company: Zimmer Medical (Shanghai) International Trading Co., Ltd.
- Manufacturing Company: Zimmer Medical (Shanghai) International Trading Co., Ltd.
- Summary: Zimmer Medical (Shanghai) International Trading Co., Ltd. initiated a voluntary Class II recall of its metal intramedullary nail surgical instruments, as announced by the National Medical Products Administration (NMPA) on July 14, 2017. The recall was prompted by concerns that the raw materials used in the affected products might be abnormal, potentially leading to an increased risk of product breakage. This proactive measure was taken by Zimmer Medical to address the identified product safety concern. The affected instruments are identified under NMPA's product registration number CFDA (Imported) No. 20131105023. Specific models, specifications, and batch details are documented in the accompanying "Medical Device Recall Event Report Form." The NMPA, as the overseeing regulatory body, facilitated the public notification of this recall to ensure patient safety and product quality standards are maintained within the medical device market. The Class II designation indicates that the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote. This recall highlights the manufacturer's responsibility in monitoring product integrity and taking corrective actions under the NMPA's oversight.

Company: https://www.globalkeysolutions.net/companies/zimmer-medical-shanghai-international-trading-co-ltd/22d50256-8f36-4c1a-ba7d-ae035c933119/