Drugs & medicalClass II

Ascend Laboratories, LLC recalls Metoprolol Succinate Extended-Release Tablets, USP 25 mg, Rx Only, 100 Tablets per bottle, Manufactured by: Alkem Laboratories Ltd.,…

Failed Dissolution Specification

Read the official notice →
Date
2023-02-01
Country
United States
Brand
Ascend Laboratories
Product
Metoprolol Succinate Extended-Release Tablets, USP 25 mg, Rx Only, 100 Tablets per bottle, Manufactured by: Alkem Laboratories Ltd.,…
Classification
Class II
Units
Nationwide and Puerto Rico
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Ascend Laboratories recalls

  1. 2023-07-26
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  3. 2023-04-26
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    Ascend Laboratories, LLC recalls Aripiprazole Tablets, USP, 20 mg, Rx Only, Packaged in 500-count bottle Manufactured by: Alkem Laboratories Ltd., INDIA Distributed by:…

    Out of specification (OOS) for Spectroscopic Identification test by IR.

    FDA · DrugAscend Laboratories, LLCNationwide in the USAOfficial notice →
  5. 2023-04-05
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    Ascend Laboratories, LLC recalls Dabigatran Etexilate 150mg Capsules, 150 mg, Rx Only, 60 Capsules per bottle, Manufactured by: Alkem Laboratories Ltd., INDIA,…

    CGMP Deviations: Detection of N-nitroso-dabigatran (NDAB) impurity levels above the Acceptable Daily Intake Limit.

    FDA · DrugAscend Laboratories, LLCNationwide in the USA.Official notice →
  7. 2023-01-25
  8. US
    Drugs & medicalClass II

    Ascend Laboratories, LLC recalls Rasagiline Mesylate Tablets 1 mg; 30 tablets in HDPE bottle; Rx only; NDC 67877-260-30; Manufactured by Alkem Laboratories Ltd., India;…

    Presence of Foreign Substance- A complaint was received of black spots/shiny metallic speck on the tablets.

    FDA · DrugAscend Laboratories, LLCCustomers in 19 states: CA, FL, GA, IL, KY, LA, MI, MN, MS, NC, NJ, NY, OH,…Official notice →
  9. 2022-02-02
  10. US
  11. 2022-01-12
  12. US
All 24 Ascend Laboratories recalls →

Other drugs & medical recalls in the United States

  1. 2023-02-01
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    Lupin Pharmaceuticals Inc. recalls Clobetasol propionate Cream USP, 0.05%, 45 g tube, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202,…

    Subpotent Drug: Low assay result observed during long-term stability testing.

    FDA · DrugLupin Pharmaceuticals Inc.USA NationwideOfficial notice →
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    Preferred Pharmaceuticals, Inc. recalls Allopurinol Tablets 100mg, USP, 90-count bottles, Rx Only, 90, Mfg: Accord Healthcare, Inc; Durham, NC, PREFERRED…

    Presence of Foreign Substance: manufacturer recalled this re-packaged product due to reports of a small piece of green plastic embedded in the crack towards the edge of the tablet.

    FDA · DrugPreferred Pharmaceuticals, Inc.INOfficial notice →
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    Accord Healthcare, Inc. recalls Allopurinol Tablets USP, 100 mg, 100-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703, Manufactured by:…

    Presence of Foreign Substance: Presence of a small piece of green plastic embedded in the crack towards the edge of the tablet.

    FDA · DrugAccord Healthcare, Inc.Nationwide in the USAOfficial notice →
  6. 2023-01-25
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    Siemens Medical Solutions USA, Inc recalls Luminos Agile Max, Luminos dRF Max, and LUMINOS Lotus Max

    There is potential for the footrest to detach from the patient table during use. Device intended to visualize anatomical structures by converting an Xray pattern into a visible image. The system has medical…

    FDA · DeviceSiemens Medical Solutions USA, IncWorldwide distributionOfficial notice →
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    R & D Systems, Inc. recalls R&D CBC-3D Hematology Control: (1) CBC-3D Normal Pack Hematology Control, REF 3D501, containing 10 x 2.0mL Control N; (2) CBC-3D TRI PACK…

    For one lot of CBC-3D Hematology Control, the Normal Level may exhibit hemolysis or deterioration due to microbial contamination.

    FDA · DeviceR & D Systems, Inc.Worldwide distribution - US Nationwide distribution in the states of CA, FL,…Official notice →
See all drugs & medical recalls →