Recall

Could cause harm

ULTRA STRENTGH, ELECTRIC MIDICATED BALM (menthol 16% and methyl salicylate 32%) packaged…

CGMP Deviations

Official FDA data record

What to do

Does your product match this recall?

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  1. 1Compare the product, size and lot or date code with this notice.
  2. 2If your product matches, stop using it and follow the official recall instructions.
  3. 3Read the official notice for return, refund or disposal instructions.

What the notice says

CGMP Deviations. This could cause temporary or reversible health problems.

Recall details

Firm
Fei Fah Medical Manufacturing Pte. Ltd.
Status
Ongoing
Reported
Nov 4, 2026
Started
Oct 23, 2026
Where sold
Nationwide within the U.S
Quantity
171,120 units
Notice number
D-0104-2027

Lots, UPC, dates

Lot: a)23FEBU7001-019, Exp. Date: October 2028; 24FEBU7001-020, Exp. Date: November 2029. b) 23FEBU1001-9, Exp. Date: October 2028; 24FEBU1001-004, Exp. Date: November 2029.

Agency wording

ULTRA STRENTGH, ELECTRIC MIDICATED BALM (menthol 16% and methyl salicylate 32%) packaged in a) Net 2.45 oz (70g) (NDC 63299-001-01) and b) 10g (NDC 63299-001-02), Manufactured by Fei Fah Medical Mfg Pte Ltd, Singapore, U.S Distributor: SOLISTICE MEDICINE COMPANY, 215 West Ann Street, Los Angeles, CA 90012

Source: FDA OTC report. This is not medical advice. Compare your package codes before you act.