Helix Pain Relieving (menthol recalls

The FDA has published 1 recall involving Helix Pain Relieving (menthol since 2023. The latest was reported on 30 Aug 2023. Most were for manufacturing (cgmp) deviations. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls1since 2023

Last 12 months0reported

Class I00% of total

Ongoing0latest 30 Aug 2023

Recalls per month, last 24 months

click a bar for that month

0Dec '24 0 0 0Mar 0 0 0Jun 0 0 0Sep 0 0 0Dec 0 0 0Mar 0 0 0Jun 0 0 0Sep 0 0

Severity split

Class I 0 0%Class II 1 100%Class III 0 0%

Why helix pain relieving (menthol is recalled

Manufacturing (CGMP) Deviations1100%

Companies

Parker Laboratories1100%

By year

20231100%

All helix pain relieving (menthol recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
30 Aug 2023Drug	CLASS II	Helix Pain Relieving Cream (Menthol 7.4%) recalled	Parker Laboratories	Manufacturing (CGMP) Deviations	Nationwide

Should you stop taking Helix Pain Relieving (menthol?

Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.