Drugs & medicalClass II

Lupin Pharmaceuticals Inc. recalls Cefdinir for Oral Suspension USP 250 mg/5 mL (60 mL when reconstituted), 60 mL bottle, Rx only, Manufactured for: Lupin…

Presence of foreign substance: Product complaint of foreign material in reconstituted bottle.

Read the official notice →
Date
2024-05-22
Country
United States
Brand
Lupin Pharmaceuticals
Product
Cefdinir for Oral Suspension USP 250 mg/5 mL (60 mL when reconstituted), 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals,…
Classification
Class II
Units
USA nationwide
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Lupin Pharmaceuticals recalls

  1. 2024-09-04
  2. US
    Drugs & medicalClass II

    Lupin Pharmaceuticals Inc. recalls Cefixime for Oral Suspension USP, 100 mg/5 mL, 50 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore,…

    Subpotent Drug- An out of specification ( OOS ) result observed in assay test during 18-month long term stability study.

    FDA · DrugLupin Pharmaceuticals Inc.USA nationwide.Official notice →
  3. 2024-06-26
  4. US
  5. 2024-06-05
  6. US
  7. 2024-04-17
  8. US
  9. 2024-02-28
  10. US
  11. 2024-02-07
  12. US
    Drugs & medicalClass II

    Lupin Pharmaceuticals Inc. recalls Rifampin Capsules USP 150mg, 30-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United…

    Subpotent Drug and Failed Impurities/Degradation Specifications

    FDA · DrugLupin Pharmaceuticals Inc.Product was distributed to 32 Wholesale/distributor accounts who further…Official notice →
All 38 Lupin Pharmaceuticals recalls →

Other drugs & medical recalls in the United States

  1. 2024-05-22
  2. US
    Drugs & medicalClass II

    Pharma Nobis LLC recalls Meijer Magnesium Citrate Saline Laxative Oral Solution Dye Free, Sugar Free Grape, 10 fl. oz bottle, Distributed by: Meijer Distribution…

    Microbial Contamination of Non-Sterile Products - Presence of Acetobacter nitrogenifigens bacteria

    FDA · DrugPharma Nobis LLCUSA NationwideOfficial notice →
  3. US
    Drugs & medicalClass II

    Sagent Pharmaceuticals recalls MethylPREDNISolone Acetate Injectable Suspension, USP, 400 mg per 10 mL (40 mg per mL), 1 x 10 mL Multi-Dose Vial, Rx only, Mfd. for…

    Presence of Particulate Matter: Potential for black particulates in the drug product.

    FDA · DrugSagent PharmaceuticalsNationwide in the USAOfficial notice →
  4. US
    Drugs & medicalClass II

    MACLEODS PHARMA USA, INC recalls Losartan Potassium and Hydrochlorothiazide Tablets, USP 50mg /12.5 mg, 1000-count bottle, Rx only, Manufactured for: Macleods Pharma…

    Presence of foreign substance: plastic-like substance.

    FDA · DrugMACLEODS PHARMA USA, INCUSA NationwideOfficial notice →
  5. US
    Drugs & medicalClass II

    Dercher Enterprises, Inc., DBA Gordon Laboratories recalls Gordofilm Wart Remover (salicylic acid 16.7% USP) packaged in 15 cc glass jars, Gordon Laboratories, Upper…

    cGMP Deviations

    FDA · DrugDercher Enterprises, Inc., DBA Gordon LaboratoriesProduct was distributed nationwide within the United StatesOfficial notice →
  6. US
    Drugs & medicalClass I

    Stop Clopez Corp recalls Schwinnng Herbal Dietary Supplement Capsules, packaged in 10-count boxes, distributed by VSD Productions Inc., Las Vegas, NV.

    Marketed Without An Approved NDA/ANDA

    FDA · DrugStop Clopez CorpDistribution worldwide via amazon.comOfficial notice →
  7. 2024-05-15
  8. US
    Drugs & medicalClass III

    Randox Laboratories Ltd. recalls Evidence MultiSTAT with software v 3.7-Analyzer intended for the qualitative determination of parent drug molecule and metabolites of…

    Foam gasket on the Evidence MultiSTAT chip heater assembly may not perform as expected. Foam that is not functioning as expected may cause light to leak into the Charged Coupled Device (CCD) Camera during imaging. This…

    FDA · DeviceRandox Laboratories Ltd.US Nationwide distribution.Official notice →
See all drugs & medical recalls →