The Recall Desk
LowFDA (Drugs)·D-1530-2019·Announced 2019-08-07

Good to Go Hand Sanitizer Recalled for Missing Stability Testing

NingBo Huize Commodity Co., Ltd. is recalling Good to Go Hand Sanitizer because stability testing was not conducted on the product.

What this means for you

Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.

Our severity reasoning: The recall is classified as FDA Class III, which indicates the product is not likely to cause adverse health consequences. The issue is a documentation and testing deviation (missing stability testing) rather than a confirmed contamination or defect causing harm.

Plain-English summary

NingBo Huize Commodity Co., Ltd. is voluntarily recalling Good to Go Hand Sanitizer (Ethyl Alcohol 62%), 1 FL OZ (30 mL), OTC. The recall is due to Current Good Manufacturing Practice (CGMP) deviations, specifically that stability testing was not conducted on the manufactured hand sanitizer product.

The affected product was made in China for Cashco Distributors Inc. The distribution pattern indicates the foreign manufacturer is located in China and the product was distributed to seven consignees located in China. The recall covers 52,160 units across five specific lot numbers with expiration dates ranging from May 31, 2020, to August 21, 2020.

Consumers who have purchased this product should stop using it and return it to the place of purchase for a refund or contact the recalling firm for further instructions.

The recalled product

Product
Good to Go Hand Sanitizer (Ethyl Alcohol 62%), 1 FL OZ (30 mL), OTC, Made in China for Cashco Distributors Inc. 6430 N. E. Columbia Blvd Portland OR 97218
Manufacturer
NingBo Huize Commodity Co.,Ltd.
Category
Drug — OTC Hand Sanitizer
Hazard
Affected units
52,160

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (5)

  • Lot #: 20180601 Exp 5/31/2020
  • 20180604 Exp 6/3/2020
  • 20180820 Exp 8/19/2020
  • 20180821 Exp 8/20/2020
  • 20180822 Exp 8/21/2020

Distribution

Distribution scope not specified by the agency.

Part of a larger recall action

This product is one of 36 recalled by NingBo Huize Commodity Co.,Ltd. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 36 products in this recall →

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