# China NMPA Product Recall - VERION Ophthalmic Biometry and Surgical Planning System (Vision Planning System)

Source: https://www.globalkeysolutions.net/records/china_product_recall/alcon-gps-wavelight-gmbh/d46a2512-4113-4939-972b-2b5506092077/
Source feed: China

> China NMPA product recall for VERION Ophthalmic Biometry and Surgical Planning System (Vision Planning System) by Alcon GPS WaveLight GmbH published May 19, 2016. Recall level: Level 3 Recall. Alcon GPS - WaveLight GmbH, in cooperation with its Chinese affiliate Alcon (China) Ophthalmic Produ

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Alcon GPS - WaveLight GmbH is proactively recalling the VERION ophthalmic biometry and surgical planning system (vision planning system).
- Company Name: Alcon GPS WaveLight GmbH
- Publication Date: 2016-05-19
- Product Name: VERION Ophthalmic Biometry and Surgical Planning System (Vision Planning System)
- Recall Level: Level 3 Recall
- Recall Reason: Unexpected curved incisions outside the surgical plan appear in printed, saved (.pdf), or exported surgical plans.
- Discovering Company: Alcon (China) Ophthalmic Products Co., Ltd.
- Manufacturing Company: Alcon GPS WaveLight GmbH
- Summary: Alcon GPS - WaveLight GmbH, in cooperation with its Chinese affiliate Alcon (China) Ophthalmic Products Co., Ltd., initiated a voluntary Class III recall for its VERION Ophthalmic Biometry and Surgical Planning System (Vision Planning System). This action, reported by the National Medical Products Administration (NMPA) on May 19, 2016, addresses a critical issue within the device. The main problem identified was the generation of "unexpected curved incisions outside the surgical plan" on printed, saved, or exported surgical plans. This significant deviation from the intended surgical blueprint could potentially compromise the accuracy of ophthalmic procedures and impact patient safety. The VERION system, registered under number 20143226003, is designed to provide precise surgical planning, making this flaw a serious functional concern. The voluntary recall demonstrates the company's proactive measure to rectify product deficiencies under the regulatory guidance of the NMPA, which oversees medical device safety and efficacy. While specific inspection dates are not detailed, the recall serves as a corrective action in response to identified product non-conformities, aligning with NMPA's framework for medical device oversight. Detailed information regarding affected product models and specifications is available in an attached Medical Device Recall Event Report Form.

Company: https://www.globalkeysolutions.net/companies/alcon-gps-wavelight-gmbh/1f2ab517-d274-4f72-89e8-5541d07a1166/