# China NMPA Product Recall - Disposable external aspiration tubing Riptide™ Large Bore Aspiration Tubing

Source: https://www.globalkeysolutions.net/records/china_product_recall/micro-therapeutics-inc-dba-ev3-neurovascular/b6b7be20-48f7-4c39-bee7-2e7bc71f8cf2/
Source feed: China

> China NMPA product recall for Disposable external aspiration tubing Riptide™ Large Bore Aspiration Tubing by Micro Therapeutics Inc. dba ev3 Neurovascular published November 21, 2025. Recall level: Level 3 Recall. Micro Therapeutics, Inc. (DBA ev3 Neurovascular) has initiated a voluntary Class III recall, reporte

---

## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Micro Therapeutics, Inc. (DBA ev3 Neurovascular) is issuing a voluntary recall for its disposable Riptide™ Large Bore Aspiration Tubing tubing.
- Company Name: Micro Therapeutics Inc. dba ev3 Neurovascular
- Publication Date: 2025-11-21
- Product Name: Disposable external aspiration tubing Riptide™ Large Bore Aspiration Tubing
- Recall Level: Level 3 Recall
- Recall Reason: Two batches of products may have incorrect use-by dates on their labels. These batches of products may have incorrect use-by dates on the packaging bags and/or cartons, which differ from the actual use-by date (3 years from the production date).
- Discovering Company: Covidien Medical Devices International Trading (Shanghai) Co., Ltd.
- Manufacturing Company: Micro Therapeutics Inc. dba ev3 Neurovascular
- Summary: Micro Therapeutics, Inc. (DBA ev3 Neurovascular) has initiated a voluntary Class III recall, reported by Covidien Medical Devices International Trading (Shanghai) Co., Ltd., for specific batches of its Riptide™ Large Bore Aspiration Tubing. This recall, published by the National Medical Products Administration (NMPA) on November 21, 2025, addresses a labeling discrepancy. The main issue involves product labels displaying incorrect, prematurely early use-by dates on packaging bags and/or cartons, differing from the actual three-year shelf life. Despite receiving five complaints by October 31, 2025, investigations confirmed that the affected products were still within their true shelf life (manufactured October 2024), ensuring no risk to patient safety. Under NMPA regulatory oversight for imported medical devices, the company is taking action to remove the mislabeled batches from circulation. Detailed information regarding affected product models, specifications, and batch numbers is provided in the "Medical Device Recall Event Report Form."

Company: https://www.globalkeysolutions.net/companies/micro-therapeutics-inc-dba-ev3-neurovascular/6f7ef542-0405-4c6a-839f-b164f7f30fac/