# China NMPA Product Recall - Disposable sterile syringe with needle

Source: https://www.globalkeysolutions.net/records/china_product_recall/yunnan-haodi-medical-equipment-co-ltd/97b3d315-f874-45b8-8fb0-a52f4e29a624/
Source feed: China

> China NMPA product recall for Disposable sterile syringe with needle by Yunnan Haodi Medical Equipment Co., Ltd. published October 19, 2021. Recall level: Level 3 Recall. On October 19, 2021, Yunnan Haodi Medical Device Co., Ltd. initiated a Class III voluntary recall fo

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Yunnan Haodi Medical Device Co., Ltd. is voluntarily recalling disposable sterile syringes with needles.
- Company Name: Yunnan Haodi Medical Equipment Co., Ltd.
- Publication Date: 2021-10-19
- Product Name: Disposable sterile syringe with needle
- Recall Level: Level 3 Recall
- Recall Reason: The business qualifications do not meet the requirements of the regulations for the operation of medical devices.
- Discovering Company: Yunnan Haodi Medical Equipment Co., Ltd.
- Manufacturing Company: Yunnan Haodi Medical Equipment Co., Ltd.
- Summary: On October 19, 2021, Yunnan Haodi Medical Device Co., Ltd. initiated a Class III voluntary recall for its disposable sterile syringes with needles. This action, reported by the company and published by the National Medical Products Administration (NMPA) and the Yunnan Provincial Drug Administration, was prompted by the product's non-compliance with established regulations governing medical device operations. While no specific inspection dates are provided in this announcement, the recall addresses a detected deviation from regulatory standards. The core issue involves a general non-adherence to the operational requirements for medical devices, which are critical for ensuring product quality and patient safety. As a required measure, Yunnan Haodi Medical Device Co., Ltd. is voluntarily withdrawing the affected syringes from distribution. Further comprehensive details concerning the specific models, specifications, and batch numbers of the recalled products are documented in a separate Medical Device Recall Event Report Form. This proactive step highlights the company’s responsibility in maintaining regulatory compliance and upholding the integrity of medical products.

Company: https://www.globalkeysolutions.net/companies/yunnan-haodi-medical-equipment-co-ltd/276cb2bd-c6d8-4484-a3c3-21db967081ed/