Drugs & medicalClass II

The Harvard Drug Group LLC recalls Omega-3-Acid, Ethyl Esters, Capsules, USP, 1 gram, 50 capsules (5 x 10 unit dose blister cards) per carton, Rx only, Packaged and…

Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells.

Read the official notice →
Date
2026-04-29
Country
United States
Brand
Harvard Drug Group
Product
Omega-3-Acid, Ethyl Esters, Capsules, USP, 1 gram, 50 capsules (5 x 10 unit dose blister cards) per carton, Rx only, Packaged and…
Classification
Class II
Units
Nationwide in the USA
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Harvard Drug Group recalls

  1. 2026-07-01
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  3. 2026-04-22
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  5. 2026-03-11
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    Defective container; inadequately sealed blister packaging.

    FDA · DrugThe Harvard Drug Group LLCNationwide US.Official notice →
  7. 2025-10-29
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    The Harvard Drug Group LLC recalls Gabapentin Capsules, USP, 100 mg, 10 Capsules (10 x 1 blister pack), Rx only, Packaged and Distributed by: Major Pharmaceuticals,…

    Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .

    FDA · DrugThe Harvard Drug Group LLCUS Nationwide.Official notice →
  9. 2025-07-09
  10. US
    Drugs & medicalClass II

    The Harvard Drug Group LLC recalls Gabapentin Capsules, USP, 100 mg, 100 capsules (10x10), blister pack cartons, Rx only, Packaged and Distributed by: MAJOR…

    Defective container; blister packaging inadequately sealed.

    FDA · DrugThe Harvard Drug Group LLCNationwideOfficial notice →
  11. 2023-07-05
  12. US
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    The Harvard Drug Group recalls Tramadol Hydrochloride Tablets, USP 50 mg, Unit Dose 100-Count Tablets Rx only, Manufactured by: Sun Pharmaceutical Industries Ltd. Survey…

    Packaging defect: blister packaging inadequately sealed.

    FDA · DrugThe Harvard Drug GroupNationwide in the U.S.Official notice →
All 12 Harvard Drug Group recalls →

Other drugs & medical recalls in the United States

  1. 2026-04-29
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    In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.

    FDA · DeviceUvlizer c/o RAIS INTERNATIONAL LLCU.S.Official notice →
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    Teva Pharmaceuticals USA, Inc recalls Claravis (isotretinoin capsule, USP), 10 mg, Packaged as a) 100-count carton, NDC 0555-1054-56, with 10x10 blister packs NDC…

    Failed Impurities/Degradation Specifications: Out of specification for specific impurity Tretinoin

    FDA · DrugTeva Pharmaceuticals USA, IncNationwide in the USA, Puerto Rico and Virgin IslandsOfficial notice →
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    B BRAUN MEDICAL INC recalls DEXTROSE INJECTION USP, 70%, 2000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7387-50.

    Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.

    FDA · DrugB BRAUN MEDICAL INCUS Nationwide.Official notice →
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    Premier Dental Products Co recalls Premier, Monsel's, Ferric Subsulfate Solution, 8 mL bottles, Rx only, Manufacturer: Premier Medical Products, 1710 Romano Drive,…

    Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14). It is important to note that this error is limited to the…

    FDA · DrugPremier Dental Products CoNationwide within the United StatesOfficial notice →
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    Lack of Assurance of Sterility

    FDA · DrugHarrow Eye LLCNationwide within the United StatesOfficial notice →
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    Leading Pharma, LLC recalls Furosemide Tablets, USP, 80 mg, 100 Tablets bottles, Rx only, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004, NDC 69315-118-01

    CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit.

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See all drugs & medical recalls →