FDA Drugs recall ·
ULTRA STRENTGH, ELECTRIC MIDICATED BALM (menthol 16% and methyl salicylate… recall
- Recall number
- D-0104-2027
- Date
- (initiated October 23, 2026)
- Company / brand
- Fei Fah Medical Manufacturing Pte. Ltd.
61 Kaki Bukit Avenue 1, Singapore, Singapore - Category
- Drugs › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 171,120 units
- Hazard tags
- Manufacturing practices (cGMP)
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
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
Why was it recalled?
CGMP Deviations
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
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.
Distribution
Nationwide within the U.S
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (drugs), recall D-0104-2027. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.