# China NMPA Product Recall - Electric hydraulic multi-functional operating table

Source: https://www.globalkeysolutions.net/records/china_product_recall/hefei-heershi-technology-development-co-ltd/e6dab5e7-619c-44a6-adc2-2b41757d2540/
Source feed: China

> China NMPA product recall for Electric hydraulic multi-functional operating table by Hefei Heershi Technology Development Co., Ltd. published August 30, 2017. Recall level: Level 3 Recall. Hefei Heersi Technology Development Co., Ltd. initiated a voluntary Class III recall for its Electri

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Hefei Heershi Technology Development Co., Ltd. voluntarily recalls its electric hydraulic multifunctional operating table.
- Company Name: Hefei Heershi Technology Development Co., Ltd.
- Publication Date: 2017-08-30
- Product Name: Electric hydraulic multi-functional operating table
- Recall Level: Level 3 Recall
- Recall Reason: The input power values on the nameplate and instruction manual do not match the values specified in the registered product technical requirements.
- Discovering Company: Hefei Heershi Technology Development Co., Ltd.
- Manufacturing Company: Hefei Heershi Technology Development Co., Ltd.
- Summary: Hefei Heersi Technology Development Co., Ltd. initiated a voluntary Class III recall for its Electric Hydraulic Multifunctional Operating Table, as announced on August 30, 2017, by the National Medical Products Administration (NMPA). The core issue identified was an inconsistency where the input power value displayed on the product's nameplate and detailed in its instruction manual did not align with the values specified in the registered product technical requirements. This discrepancy indicated a misrepresentation in the official documentation and labeling of the device's electrical specifications. While specific inspection dates were not provided, the recall itself served as a regulatory notification of non-compliance. Hefei Heersi was required to voluntarily remove the affected products from circulation. Further information regarding the specific models, specifications, and batches involved in the recall was made available in a dedicated Medical Device Recall Event Report Form. The Class III classification suggests that the use of or exposure to the recalled product is not expected to cause significant adverse health consequences.

Company: https://www.globalkeysolutions.net/companies/hefei-heershi-technology-development-co-ltd/53617e8b-4806-4677-baa4-428a93c2b841/