Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class III · Low risk Terminated Initiated Apr 1, 2019 (8 years ago)

Lemon Hand Sanitizer

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products.

Cause type: Stability / shelf life

The product degraded or failed stability testing before its labeled expiry. Heat, moisture or time can break the drug down into degradants or reduce potency. All stability / shelf life recalls.

What was recalled

Lemon Hand Sanitizer (Alcohol 62%), 30 mL / 1.0 fl.oz, OTC, Made in China.

Drug: Alcohol

Recalling firm
NingBo Huize Commodity Co.,Ltd.
Origin
N/A, China
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1564-2019 · FDA notice

Low risk, still worth a check. Class III means the product is unlikely to cause harm but breaks an FDA rule (often labeling). If your lot matches, your pharmacy will normally swap it; there is no need for alarm. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other Alcohol recalls

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Other recalls by NingBo Huize Commodity Co.,Ltd.

All 2019 recalls