FDA-Drug2026-10-27Class IIPROCESSING DEFECT
Fei Fah Electric Medicated Balm recalled over manufacturing issues
What this means
Fei Fah Medical Manufacturing recalled its Ultra Strength Electric Medicated Balm because it did not meet FDA manufacturing quality standards (CGMP). The recall covers about 171,120 units sold nationwide in 70g and 10g sizes. No injuries have been reported.
- Check the NDC (63299-001-01 or 63299-001-02) and lot numbers on the package against the recall notice.
- If they match, stop using the product and keep it out of reach of children and pets.
- Contact the U.S. distributor, Solistice Medicine Company, for return or refund instructions.
The agency's original wording
Hazard
CGMP Deviations
Intended for
All ages (under 0 months)
Illnesses reported
None reported
Sold states
Nationwide within the U.S
Affected count
171,120 units
Manufactured in
61 Kaki Bukit Avenue 1, #02-29 Shun Li Industrial Park, Singapore, Singapore
Products
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
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0104-2027Want us to check the next one for you?
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