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Recalls Watch

FDA recall 100211: Fei Fah Medical Manufacturing Pte. Ltd.: ULTRA STRENTGH

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FDARecall 100211Medicines

What to do

The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Talk to your pharmacist or doctor before stopping a medicine.Note from Recalls Watch, not agency text.

Read the official notice on accessdata.fda.gov (opens in a new tab)

Hazard

Why it was recalled

CGMP Deviations
Text from FDA, unedited.

FDA classification: Class II. Use may cause temporary or medically reversible health consequences, or the chance of serious consequences is remote. Status: Ongoing.

Is it yours? Products and codes

Type the lot, batch, date code, model number or UPC printed on the product. It is compared here, in your browser, with the codes this notice lists. The code is also added to the page address (?lot=…), so a copied link or result carries it.

General information on recalls from the agency: U.S. Food and Drug Administration (opens in a new tab).

  • 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

    Lot or code
    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.
    FDA recall number
    D-0104-2027
    Quantity
    171,120 units

Distribution (FDA): Nationwide within the U.S

About this record

Issued by
U.S. Food and Drug Administration
Firm
Fei Fah Medical Manufacturing Pte. Ltd.
Title
Composed by Recalls Watch from fields of the record; FDA records have no title.

If someone was hurt or swallowed something: call 911, or Poison Help at 1-800-222-1222.

Checking this recall, step by step

Four steps, in this order. Nothing on this page replaces the advice of the agency or of your pharmacist, doctor or dealer.

  1. Read the lot, code or model printed on your package and compare it with the codes in “Is it yours?” below.
  2. Read the instruction under “What to do” and the firm contact above; the official notice is the reference for what to do with that bottle.
  3. Open the official notice to confirm the current text: agencies can update a recall after this page was collected.
  4. Copy, share or print the notice for the pharmacy, the store, the dealer or the family member who owns the product.

Other notices that name ultra

Titles in the catalog that contain the same product word, from any firm. Compare the firm and the codes: a different firm or lot is a different recall.

Directory and lookup links

Check all notices from this recalling firm in the directory of recalls by brand and manufacturer. Browse more medicines recalls, or check another notice by its number in the recall number lookup.

About this recall

What is the hazard?

FDA states: “CGMP Deviations”

What should I do if I have this product?

The FDA record of this recall has no instruction for consumers. Compare the lot codes on the notice with your product and follow the notice of the firm. The official report is linked on this page.

How do I know if my product is included?

Compare the lot or code printed on your product with the codes FDA lists on this notice, product by product.

How does the code check on this page work?

You type the lot, batch, date code, model number or UPC from your package and the page compares it, in your browser, with the codes FDA lists on this notice. It reports a match, a possible match (your code is part of a longer listed code) or no match. It only compares text: a notice that describes products by dates, sizes or “all lots” cannot be compared, so “no match” does not clear a product. The comparison runs in your browser and the page does not send the code anywhere, but the code is added to the page address (?lot=…): a link you copy, share or bookmark carries it, and whoever opens that link requests that address from this site.

When was this recall published?

FDA published recall 100211 on November 4, 2026.

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