Recall Atlas
Drugs & medicalClass I

Lohxa, LLC recalls SENNA Syrup (sennosides) 8.8 mg/ 5 mL unit-dose cups, packaged in 24 cups per carton, Mfg for: AvKARE, TN 38478, NDC 50262-731-24.

Microbial Contamination of Non-Sterile Product

Read the official notice →
Date
2022-01-26
Country
United States
Brand
Lohxa, LLC
Product
SENNA Syrup (sennosides) 8.8 mg/ 5 mL unit-dose cups, packaged in 24 cups per carton, Mfg for: AvKARE, TN 38478, NDC 50262-731-24.
Classification
Class I
Units
Product was distributed to one wholesale who further distributed the product…
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2022-01-26
  2. US
    Drugs & medicalClass III

    Dr. Reddy's Laboratories, Inc. recalls Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into cartons,…

    Subpotent drug

    FDA · DrugDr. Reddy's Laboratories, Inc.USA NationwideOfficial notice →
  3. US
    Drugs & medicalClass II

    Mayne Pharma Inc recalls Lexette (halobetasol propionate) Topical Foam, 0.05% 50 g canisters, Rx ONLY, Distributed by: Mayne Pharma Greenville, NC 27834, NDC…

    CGMP Deviation: Difficulty dispensing/does not dispense or dispensing liquid instead of foam.

    FDA · DrugMayne Pharma IncNationwide within the United StatesOfficial notice →
  4. US
    Drugs & medicalClass III

    Dr. Reddy's Laboratories, Inc. recalls QC QUALITY CHOICE, Fexofenadine HCl 60mg and Pseudoephedrine HCl 120mg, Extended-Release Tablets, USP, Allergy & Congestion, 10…

    Failed Dissolution Specifications

    FDA · DrugDr. Reddy's Laboratories, Inc.Nationwide in the USAOfficial notice →
  5. US
    Drugs & medicalClass II

    VistaPharm, Inc. recalls Clobazam Oral Suspension 2.5 mg/mL, 120 mL bottles, Rx only, Manufactured by: VistaPharm, Inc. Largo, FL 33771, NDC 66689-058-04

    Failed Stability Specifications

    FDA · DrugVistaPharm, Inc.Nationwide within the United States including Puerto RicoOfficial notice →
  6. US
    Drugs & medicalClass II

    Ingenus Pharmaceuticals Llc recalls Clobetasol Propionate Foam, 0.05%, packaged in a) 50 g can (NDC 50742-304-50), and b) 100 g can (NDC 50742-304-01), Rx only,…

    CGMP Deviations

    FDA · DrugIngenus Pharmaceuticals LlcNationwide in the USAOfficial notice →
  7. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA recalls Brinzolamide Ophthalmic Suspension, USP 1%, packaged as a)10 ml dropper bottles (NDC 0591-2127-79), and b) 15 ml dropper bottles (NDC…

    Defective Container: The notch in the cap that fits into the nozzle of the dropper could break off and block the dropper possibly resulting in the product not dispensing.

    FDA · DrugTeva Pharmaceuticals USANationwide in the USAOfficial notice →
See all drugs & medical recalls →