# China NMPA Product Recall - A.T.S. Cuffs

Source: https://www.globalkeysolutions.net/records/china_product_recall/zimmer-surgical-inc/d1bb54ab-d190-4505-91ce-1da80436b4e9/
Source feed: China

> China NMPA product recall for A.T.S. Cuffs by Zimmer Surgical, Inc. published January 15, 2020. Recall level: Level 2 Recall. On January 15, 2020, the National Medical Products Administration (NMPA) publicly announced a Class 

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Zimmer Surgical, Inc. is proactively recalling its A.T.S. Cuffs.
- Company Name: Zimmer Surgical, Inc.
- Publication Date: 2020-01-15
- Product Name: A.T.S. Cuffs
- Recall Level: Level 2 Recall
- Recall Reason: There may be a potential leakage issue between two airbags in certain product models and batches.
- Discovering Company: Zimmer Medical (Shanghai) International Trading Co., Ltd.
- Manufacturing Company: Zimmer Surgical, Inc.
- Summary: On January 15, 2020, the National Medical Products Administration (NMPA) publicly announced a Class II voluntary recall initiated by Zimmer Surgical, Inc. This critical action concerns specific models and batches of the company's A.T.S. Cuffs, identified under Registration Certificate No.: 20142146077. The recall was reported by Zimmer (Shanghai) Medical International Trading Co., Ltd. The core issue driving this recall is a potential leakage problem discovered between two cuffs in a particular model and batch of the devices. Such a defect could compromise the intended function and safety of the medical product. Operating within the regulatory framework established by the NMPA, Zimmer Surgical, Inc. is required to remove these potentially faulty devices from circulation. A Class II recall signifies that the use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote. The company's immediate action involves identifying and withdrawing all affected products. Comprehensive details regarding the specific models, specifications, and batch numbers subject to this recall are provided in the "Medical Device Recall Event Report Form," which accompanies the NMPA's official announcement. This voluntary recall underscores the manufacturer's responsibility to maintain product quality and adhere to safety standards under regulatory scrutiny.

Company: https://www.globalkeysolutions.net/companies/zimmer-surgical-inc/3ffd957e-b25a-4504-a499-ab6d05dec0c0/