Heritage Pharmaceuticals Inc Clindamycin Palmitate Hydrochloride FOR Oral Solution recall: Presence of Foreign Substance: presence of particles and white flakes
Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles.
The hazard: Foreign material — foreign objects
This is a foreign-material recall — foreign objects where there should be none. An affected pack looks identical to a sound one from the outside.
What the notice says: Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles.
Why it matters: Pieces of foreign objects may be inside the product. The risk here is physical rather than microbial: cuts to the mouth or throat, a broken tooth, or an injury further down if a fragment is swallowed.
Symptoms and when to call a doctor
If someone has swallowed a fragment and has mouth or throat pain, trouble swallowing, chest or stomach pain, vomiting, or blood in saliva or stool, they should be seen the same day. A fragment swallowed without symptoms usually passes on its own, but tell the clinician exactly what the product was: whether it shows up on imaging depends entirely on the material, so describe the product and the notice to them.
This page is general information, not medical advice. If you feel unwell, a clinician who can see you is the only person able to judge your case.
Recall details
- Recall number
- D-0768-2026
- Published
- August 19, 2026
- Risk level
- Class II
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- Heritage Pharmaceuticals Inc
- Product type
- Prescription & OTC drugs
- Distribution
- Nationwide
- Made in
- United States
- Lot / code info
- Lot #: 2411550, Exp. 2026/NOV.
Products covered by this recall
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
Check your product
The notice names 9 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.
Lot or batch code
Usually ink-stamped near the seam, the cap or the bottom of the pack.
- 2411550
- Exp. 2026
- NOV
Best-by / use-by date
Printed beside the lot code, not on the price sticker.
- 2026
- NOV
NDC number
On the carton and again on the bottle or blister label.
- 23155-603-51
Package size
Match the net weight or the piece count on the front of the pack.
- 75 mg
- 5 mL
- 100 mL
Codes are lifted verbatim from the FDA — Drug enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.
What to do about Foreign material
Heritage Pharmaceuticals Inc — This is a foreign-material recall — foreign objects where there should be none. An affected pack looks identical to a sound one from the outside.
- Stop eating it, and do not pick through it to find the fragment — sorting it by hand is how people get cut.
- Return it to the store or bin it sealed, and claim the refund using the lot code from the label.
- Check the freezer and the pantry for other packs carrying the same codes before you consider the matter closed.
- If someone has already bitten into something hard, have them stop, spit out what is in their mouth and rinse rather than swallow.
Getting a refund without the pack
The commonest reason people skip the refund is that they have already thrown the item away. That rarely matters.
- A photo of the label and lot code is accepted by most grocers, and so is a card statement line showing the purchase.
- Store credit is often offered first. You can ask for the original payment method instead, and it is normally granted.
- No photo either? Ask anyway. Grocery chains settle recall refunds at the service desk because disputing them costs more than paying them.
- For a multi-pack or a case, ask for the full purchase price rather than a per-unit figure — the recall covers what you paid.
Company contact: Heritage Pharmaceuticals Inc — 1 Tower Center Blvd Ste 1700, East Brunswick, NJ, 08816-1145
The official notice
This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.
Open the FDA — Drug enforcement record U.S. Food and Drug Administration recalls
Questions people ask about this recall
Why was Heritage Pharmaceuticals Inc prescription & otc drugs recalled?
Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles. Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles.
How do I know if I have the recalled product?
Match the codes printed on your package against the notice: lot code 2411550, Exp. 2026, NOV; best-by date 2026 or NOV. If the code on your package is not on that list, your unit is outside the recall.
What should I do with it right now?
Stop eating it, and do not pick through it to find the fragment — sorting it by hand is how people get cut.
Can I get my money back?
A photo of the label and lot code is accepted by most grocers, and so is a card statement line showing the purchase.
Where was the recalled product sold?
It was distributed nationwide.
Related recalls
-
Class II · 12 months ago
Heritage Pharmaceuticals Inc Desipramine Hydrochloride Tablets, USP, 25 mg recall: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
-
Class II · 12 months ago
Heritage Pharmaceuticals Inc Desipramine Hydrochloride Tablets, USP, 150 mg recall: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
-
Class II · 12 months ago
Heritage Pharmaceuticals Inc Desipramine Hydrochloride Tablets, USP, 10 mg recall: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
-
Class II · 12 months ago
Heritage Pharmaceuticals Inc Desipramine Hydrochloride Tablets, USP, 50 mg recall: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
-
Class II · 12 months ago
Heritage Pharmaceuticals Inc Desipramine Hydrochloride Tablets, USP, 100 mg recall: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
-
Class II · 12 months ago
Heritage Pharmaceuticals Inc Desipramine Hydrochloride Tablets, USP, 75 mg recall: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.