# China NMPA Product Recall - Distal Access Catheter

Source: https://www.globalkeysolutions.net/records/china_product_recall/microvention-inc/d33d92f5-5ed2-4ab6-8fa3-b9f3cb1b8b0c
Source feed: China

> China NMPA product recall for Distal Access Catheter by MicroVention, Inc. published July 04, 2023. Recall level: Level 3 Recall. The National Medical Products Administration (NMPA) published an announcement on July 4, 2023, regar

---

## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: MicroVention, Inc. is proactively recalling distal access catheters.
- Company Name: MicroVention, Inc.
- Publication Date: 2023-07-04
- Product Name: Distal Access Catheter
- Recall Level: Level 3 Recall
- Recall Reason: The manufacturer's name on the label of a specific batch of products destined for a specific country or region is incorrect.
- Discovering Company: Beijing Weixian Medical Technology Co., Ltd.
- Manufacturing Company: MicroVention, Inc.
- Summary: The National Medical Products Administration (NMPA) published an announcement on July 4, 2023, regarding a voluntary Class III recall initiated by MicroVention, Inc. This action was reported by Beijing MicroVention Medical Technology Co., Ltd. The recall pertains to specific batches of Distal Access Catheters due to an identified error: an incorrect manufacturer name was printed on the product labels. These affected batches were distributed to various countries and regions. While specific inspection dates were not detailed, this incident highlights the critical importance of precise labeling for medical devices. The NMPA's regulatory framework designates Class III recalls for situations where the probability of adverse health consequences is low, yet regulatory non-compliance necessitates corrective measures. The mislabeling of the manufacturer's name, even without directly compromising device function, could create ambiguity regarding product origin and regulatory accountability. The required actions involve the removal of these specific products from distribution. Comprehensive information detailing the affected models, specifications, and batch numbers is provided in an attached "Medical Device Recall Event Report Form," enabling all parties to manage the affected inventory effectively and ensure adherence to established medical device regulations.

Company: https://www.globalkeysolutions.net/companies/microvention-inc/f8e8b08c-8ab2-4598-a0b1-5486191a3716