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Unrated Drug recall · FDA · Published July 30, 2026

Heritage Pharma Recalls Clindamycin Oral Solution Due to Foreign Particles

Heritage Pharmaceuticals recalls Clindamycin Palmitate Oral Solution (75 mg/5 mL) due to foreign particles and white flakes. Check lot #2411550.

🇺🇸 FDA recall #D-0768-2026DrugHeritage Pharmaceuticals ›
✎ GovInfoNow plain-language explainer

Heritage Pharmaceuticals is recalling one lot of Clindamycin Palmitate Hydrochloride for Oral Solution because reconstituted bottles contain visible particles and white flakes. This product was distributed nationwide by Avet Pharmaceuticals. The record does not specify the exact health risks or a remedy for consumers. Read more at govinfonow.com/recall/454405-heritage-pharma-recalls-clindamycin-oral-solution-due-to-foreign-particles.

Source Summary by GovInfoNow · govinfonow.com/recall/454405-heritage-pharma-recalls-clindamycin-oral-solution-due-to-foreign-particles · Updated October 9, 2026 · FDA enforcement record: FDA #D-0768-2026

Cite this page

“Heritage Pharma Recalls Clindamycin Oral Solution Due to Foreign Particles.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/454405-heritage-pharma-recalls-clindamycin-oral-solution-due-to-foreign-particles. Based on FDA recall #D-0768-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0768-2026%22&limit=1).

Heritage Pharmaceuticals Inc voluntarily recalled Clindamycin Palmitate Oral Solution on July 30, 2026, after the FDA announced the presence of foreign particles and white flakes in reconstituted bottles. The Food and Drug Administration issued the recall notice for the Class II violation.

How to tell if you have it

  • Brand: Heritage Pharmaceuticals
  • Product: 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 #: 2411550
  • Expiration: 2026/NOV

The hazard

The recall addresses the presence of particles and white flakes in the reconstituted bottles. The FDA classified this as a Class II recall due to the foreign substance risk.

Context

GovInfoNow's records show Heritage Pharmaceuticals Inc has 11 other recalls on record since 2015-02-25. Other recent recalls include a 2025-10-06 Desipramine Tablets recall for N-Nitroso Impurity Risk, a 2022-11-23 Desmopressin Tablets recall for Subpotent Drug Risk, and a 2021-04-21 Acyclovir Tablets recall for Missing Lot/Exp Date. Other recent recalls of similar products include SUN PHARMACEUTICAL Clindamycin Phosphate Topical Solution Recall (2025-11-26) and Baxter Clindamycin Injection Recalls (2026-08-06).

How to tell if you have this one

Check your bottle for Clindamycin Palmitate Hydrochloride for Oral Solution, USP, 75 mg/5 mL. Look for NDC 23155-603-51 and Lot #2411550 with an expiration date of November 2026.

  • Brand
    Heritage Pharmaceuticals
  • Category
    Drug

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide within the U.S” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 20 days after the firm started it.

1. Firm started the recall: Jul 30, 202612. FDA classified it Class II: Aug 14, 202623. Published in FDA’s Enforcement Report: Aug 19, 202634. Added to GovInfoNow: Aug 27, 202642026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0768-2026 (July 30, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0768-2026 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA