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# FDA Says Haimen Shengbang Container Recall Class 1
- URL: https://www.fdaweb.com/fda-says-haimen-shengbang-container-recall-class-1/
- Published: 2022-08-09T12:00:00.000Z
- Updated: 2026-09-14T17:55:13.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5152471

FDA says the 7/12 Haimen Shangbang Laboratory Equipment Co. recall of 4,165,200 viral transport media containers that were distributed in the U.S. between 10/8/21 and 2/15/22 is Class 1\. An agency [notice](https://www.fda.gov/medical-devices/medical-device-recalls/haimen-shengbang-laboratory-equipment-co-ltd-recalls-viral-transport-media-containers-are-not?utm%5Fmedium=email&utm%5Fsource=govdelivery) says the company recalled the products because they were distributed to U.S. customers without authorization, clearance, or approval from FDA.

“This means there is a risk for false negative, false positive, or misinterpretation of results if these products are used to detect SARS-CoV-2,” the notice says. “Use of these products may cause serious adverse health consequences or death.”