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FDA recall 99526: Heritage Pharmaceuticals Inc: CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION

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FDARecall 99526Medicines

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

Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles.
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

  • CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION, USP, 75 mg/5 mL, Rx Only, 100 mL, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, NDC 23155-603-51

    Lot or code
    Lot #: 2411550, Exp. 2026/NOV.
    FDA recall number
    D-0768-2026

Distribution (FDA): Nationwide within the U.S

About this record

Issued by
U.S. Food and Drug Administration
Firm
Heritage Pharmaceuticals Inc
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.

About this recall

What is the hazard?

FDA states: “Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles.”

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.

When was this recall published?

FDA published recall 99526 on August 19, 2026.

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