Drugs & medicalClass II

Aurolife Pharma, LLC recalls Glycopyrrolate Tablets, USP, 1 mg, 100 tablets, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, NDC…

Failed Impurities/Degradation Specifications

Read the official notice →
Date
2022-12-28
Country
United States
Brand
Aurolife Pharma
Product
Glycopyrrolate Tablets, USP, 1 mg, 100 tablets, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, NDC…
Classification
Class II
Units
Nationwide in the USA 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Aurolife Pharma recalls

  1. 2023-06-28
  2. US
    Drugs & medicalClass III

    Aurolife Pharma, LLC recalls Glycopyrrolate Tablets, USP, 1 mg, 100-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, NDC…

    Failed Impurities/Degradation Specifications

    FDA · DrugAurolife Pharma, LLCNationwide within the United StatesOfficial notice →
  3. 2022-04-06
  4. US
    Drugs & medicalClass II

    Aurolife Pharma, LLC recalls Glycopyrrolate Tablets, USP, 1 mg, 100-count bottle, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road,…

    Presence of Foreign Substance: Complaint for pieces of glass discovered in a sealed bottle which came from equipment within the packaging room.

    FDA · DrugAurolife Pharma, LLCNationwide in the USA and Puerto RicoOfficial notice →
All 3 Aurolife Pharma recalls →

Other drugs & medical recalls in the United States

  1. 2022-12-28
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    GE Medical Systems, LLC recalls Centricity Universal Viewer 6.0. Used to display medical images (Including mammograms) and data from various imaging sources.

    There is the potential that after installation of the IAS tool, some studies can remain hidden without user notification. Access to those hidden studies requires GE Healthcare assistance, which can result in a delay in…

    FDA · DeviceGE Medical Systems, LLCNationwide distribution to CA, CO, DE, FL, IA, IL, MA, MI, MN, MO, MS, MT, ND,…Official notice →
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    CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.

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    SUN PHARMACEUTICAL INDUSTRIES INC recalls Oxcarbazepine Tablets 600mg, packaged in a) 100- count bottles (NDC 62756-185-88), b) 500-count bottles (NDC 62756-185-13),…

    Presence of foreign substance

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide within the United StatesOfficial notice →
  6. 2022-12-21
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    Cordis US Corp recalls Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection into the patient.

    There is a potential for separation at the male connector.

    FDA · DeviceCordis US CorpNationwide distribution to AZ, CA, DC, FL, GA, KY, LA, MD, MS, NY, OH, TX, WV,…Official notice →
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    A reconstruction error may occur when using the Catheter Bending functionality in Applicator Modeling or Implant Modeling

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