# China NMPA Product Recall - Hip prosthesis

Source: https://www.globalkeysolutions.net/records/china_product_recall/zimmer-medical-shanghai-international-trading-co-ltd/c975f673-8020-46dc-b1bc-fe58df599498/
Source feed: China

> China NMPA product recall for Hip prosthesis by Zimmer Medical (Shanghai) International Trading Co., Ltd. published March 16, 2020. Recall level: Level 2. Zimmer Medical (Shanghai) International Medical Trading Co., Ltd. has initiated a voluntary Level II

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Zimmer Medical (Shanghai) International Trading Co., Ltd. is voluntarily recalling hip prostheses.
- Company Name: Zimmer Medical (Shanghai) International Trading Co., Ltd.
- Publication Date: 2020-03-16
- Product Name: Hip prosthesis
- Recall Level: Level 2
- Recall Reason: The affected batch may contain items where the neck length on the product label does not match the etching on the implant.
- Discovering Company: Zimmer Medical (Shanghai) International Trading Co., Ltd.
- Manufacturing Company: Zimmer Medical (Shanghai) International Trading Co., Ltd.
- Summary: Zimmer Medical (Shanghai) International Medical Trading Co., Ltd. has initiated a voluntary Level II recall for certain batches of its hip prostheses, identified under Registration Certificate No.: 20183461567. This significant action, publicly announced by the National Medical Products Administration (NMPA) on March 16, 2020, and further detailed by the Shanghai Municipal Drug Administration, followed a thorough product complaint investigation. The primary issue discovered was a critical discrepancy between the information presented on the product label and the physical attributes of the implant. Specifically, the neck length indicated on the product packaging did not accurately match the etching found on the actual hip prosthesis. Such a mismatch could potentially lead to incorrect product selection or use, thereby posing risks to patient safety during surgical procedures. In response to this finding, Zimmer Medical has taken the required action of conducting a Level II recall to address the non-conforming products. The company is mandated to ensure proper retrieval and management of all affected units. Comprehensive details regarding the specific models, specifications, and batch numbers involved in this recall are provided in the accompanying "Medical Device Recall Event Report Form." This incident highlights the stringent regulatory oversight by bodies like the NMPA in ensuring the accuracy of medical device information and maintaining high standards for patient care.

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