# China NMPA Product Recall - ArcticGel Pads for Medical Temperature Control

Source: https://www.globalkeysolutions.net/records/china_product_recall/medivance-inc/b3a37208-2511-461f-be84-eb84f053e917/
Source feed: China

> China NMPA product recall for ArcticGel Pads for Medical Temperature Control by Medivance Inc. published February 20, 2024. Recall level: Level 1 Recall. Medivance Inc. has initiated a voluntary Class I recall of its ArcticGel Pads, which are medical tem

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Medivance Inc. is voluntarily recalling its medical temperature-controlled blankets.
- Company Name: Medivance Inc.
- Publication Date: 2024-02-20
- Product Name: ArcticGel Pads for Medical Temperature Control
- Recall Level: Level 1 Recall
- Recall Reason: The design flow rate of the neonatal medical temperature-controlled blanket differs from the instruction manual, which may affect the product's heating or cooling function.
- Discovering Company: Bard Medical Technology (Shanghai) Co., Ltd.
- Manufacturing Company: Medivance Inc.
- Summary: Medivance Inc. has initiated a voluntary Class I recall of its ArcticGel Pads, which are medical temperature control blankets. This action follows the identification of a significant issue concerning a discrepancy between the product's design flow rate and the specifications detailed in its instruction manual. The core concern is that this inconsistency may adversely affect the intended heating or cooling capabilities of the blankets, particularly for neonatal applications. The National Medical Products Administration (NMPA) published details of this recall on February 20, 2024, after the issue was reported by Bad Medical Technology (Shanghai) Co., Ltd. The Class I classification signifies that there is a reasonable probability that use of or exposure to a violative product will cause serious adverse health consequences or death. While specific inspection dates are not provided in this document, the recall itself is a proactive measure by the manufacturer in response to the identified product deficiency. The recalled products are identified under National Medical Device Registration Certificate No. 20202090509. The full scope of affected models, specifications, and batch numbers are available in the accompanying "Medical Event Report Form." Medivance Inc. is undertaking this recall to ensure patient safety and product efficacy. This situation underscores the critical importance of accurate product documentation and design adherence in the medical device industry.

Company: https://www.globalkeysolutions.net/companies/medivance-inc/43b921b2-67ea-4e4f-a653-5e583521e95f/