# China NMPA Product Recall - Soft hydrophilic contact mirror

Source: https://www.globalkeysolutions.net/records/china_product_recall/coopervision-inc/b6b16324-93e8-496e-9d0a-8ed53bab3222/
Source feed: China

> China NMPA product recall for Soft hydrophilic contact mirror by CooperVision Inc. published February 21, 2023. Recall level: Level 3 Recall. On February 21, 2023, the National Medical Products Administration (NMPA) announced a significant pr

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: CooperVision Inc. is voluntarily recalling soft hydrophilic contact lenses.
- Company Name: CooperVision Inc.
- Publication Date: 2023-02-21
- Product Name: Soft hydrophilic contact mirror
- Recall Level: Level 3 Recall
- Recall Reason: Foreign objects were found in the blister packaging.
- Discovering Company: CooperVision Products Trading (Shanghai) Co., Ltd.
- Manufacturing Company: CooperVision Inc.
- Summary: On February 21, 2023, the National Medical Products Administration (NMPA) announced a significant product recall event concerning soft hydrophilic contact lenses manufactured by CooperVision Inc. The recall was voluntarily initiated by CooperVision Inc. and reported by its subsidiary, CooperVision Products Trading (Shanghai) Co., Ltd. The critical issue prompting this action is the discovery of foreign objects within the blister packaging of specific models and batches of the contact lenses. This defect, identified in products registered under Certificate No. 20153162423, raises potential concerns regarding product quality and user safety. Operating under the NMPA's regulatory framework for medical devices, CooperVision has classified this as a Class III recall. This classification indicates that while the issue may not pose an immediate serious health threat, it warrants corrective action to prevent potential adverse outcomes. The company's proactive measure underscores its commitment to compliance and consumer protection. As a required action, CooperVision is actively retrieving the affected products from the market. Further detailed information, including specific product models, specifications, and batch numbers subject to the recall, is available in the accompanying 'Medical Device Recall Event Report Form'. This ensures that distributors and consumers can accurately identify and manage any affected items they may possess, adhering to the established recall protocols to safeguard public health.

Company: https://www.globalkeysolutions.net/companies/coopervision-inc/ab8eedee-5dce-4363-b41f-8184836e301d/