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Glenmark Pharmaceuticals Inc., USA

Glenmark Pharmaceuticals Inc., USA Recalls

All product recalls associated with Glenmark Pharmaceuticals Inc., USA.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 5141–5160 of 21320 recalls

Aspirin Dipyridamole Capsules (Glenmark) – Capsule Breakage (2022)

Failed Tablet/Capsule Specification : Capsule breakage

Class IIILow

FDAJun 29, 2022Nationwide• Glenmark Pharmaceuticals Inc., USA

A&D Diaper Rash Ointment (Mckesson) – Storage Temperature Deviation (2022)

CGMP Deviations: products were stored outside the drug label specifications.

Class IIModerate

FDAJun 29, 2022Nationwide• Mckesson Medical-Surgical Inc. Corporate Office

Bisacodyl Suppositories (Mckesson) – Storage Deviation (2022)

CGMP Deviations: products were stored outside the drug label specifications.

Class II

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Moderate

FDAJun 29, 2022Nationwide• Mckesson Medical-Surgical Inc. Corporate Office

Pataday Once Daily Relief Eye Drops (Mckesson) – Storage Deviation (2022)

CGMP Deviations: products were stored outside the drug label specifications.

Class IIModerate

FDAJun 29, 2022Nationwide• Mckesson Medical-Surgical Inc. Corporate Office

Eye-Stream Eye Wash Solution (Mckesson) – Storage Deviation (2022)

CGMP Deviations: products were stored outside the drug label specifications.

Class IIModerate

FDAJun 29, 2022Nationwide• Mckesson Medical-Surgical Inc. Corporate Office

Alcohol Swabsticks Antiseptic (Mckesson) – Storage Deviation (2022)

CGMP Deviations: products were stored outside the drug label specifications.

Class IIModerate

FDAJun 29, 2022Nationwide• Mckesson Medical-Surgical Inc. Corporate Office

Systane Eye Drops (Mckesson) – Storage Deviation (2022)

CGMP Deviations: products were stored outside the drug label specifications.

Class IIModerate

FDAJun 29, 2022Nationwide• Mckesson Medical-Surgical Inc. Corporate Office

Sterile Alcohol Prep Pads (Mckesson) – Storage Deviation (2022)

CGMP Deviations: products were stored outside the drug label specifications.

Class IIModerate

FDAJun 29, 2022Nationwide• Mckesson Medical-Surgical Inc. Corporate Office

Miralax Powder Laxative (Mckesson) – Storage Deviation (2022)

CGMP Deviations: products were stored outside the drug label specifications.

Class IIModerate

FDAJun 29, 2022Nationwide• Mckesson Medical-Surgical Inc. Corporate Office

BIOPHEN UFH Control Plasma (Aniara Diagnostica) – Incorrect Product Labeling (2022)

Incorrect product labeling was included in the package.

Low

FDAJun 28, 2022IL, IN, MI• Aniara Diagnostica LLC

Atellica CH Iron_2 (Siemens Healthcare) – Falsely Elevated Results (2022)

Falsely Elevated Atellica CH Microalbumin_2 (ALB_2) Results due to Reagent Carryover from the Iron_2 Assay. This defect occurs only when a microalbumin test is run immediately after an iron test.

Moderate

FDAJun 28, 2022Nationwide• Siemens Healthcare Diagnostics, Inc.

ChemoLock Bag Spike (ICU Medical) – Port Connection Variation (2022)

Ports have a potential for unintended disconnection, inability to connect to or fully engage with injectors, due to a variation in the spring inside the Port, which may cause delay of therapy and exposure to caustic substances. Ports available as standalone connectors, or utilized as access points on vial adaptors, bag spikes, and administration sets.

Moderate

FDAJun 27, 2022Nationwide• ICU Medical, Inc.

HAMILTON-C6 Intensive Care Ventilator (Hamilton Medical) – Status Board Water Risk (2022)

Ventilator status indicator board can become loose, which could lead to water ingress (disinfectants) that may lead to technical fault alarms. Multiple technical faults in a short time may force ventilators into Safety Ventilation (blower runs constantly) or Ambient Sate (inspiratory channel/expiratory valves opened; patient breaths room air unassisted) with Panel connection lost message displayed

Moderate

FDAJun 27, 2022Nationwide• Hamilton Medical AG Via Crusch 8 Bonaduz Switzerland

Divalproex Sodium Tablets 500mg (Sun Pharmaceutical) – Dissolution Failure (2022)

Failed Dissolution Specifications: Failure occurred during routine stability testing of dissolution test.

Class IIModerate

FDAJun 27, 2022Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Za'atar Seasoning (Fuchs) – Salmonella contamination (2022)

Salmonella

The product may be potentially positive for Salmonella due to one of the sub-ingredients (oregano) testing positive for Salmonella.

Class IHigh

FDAJun 27, 2022PA• Fuchs North America, Inc.

Daytrana Patch (Noven) – Delivery System Defect (2022)

Defective Delivery System: Customer complaints received for ripping patches and tight release/adhesive transfer.

Class IIModerate

FDAJun 24, 2022Nationwide• Noven Pharmaceuticals Inc

Medline Sprinter OTW (Medtronic) – Incorrect Balloon Diameter Print (2022)

Luer has balloon diameter printed as "2.25mmx12mm" instead of the correct diameter, "2.5mmx12mm" as reflected on the product outer packaging.

Low

FDAJun 24, 2022Nationwide• Medtronic Inc

Ambra PACS Software (DICOM Grid) – Patient Information Edit Issue (2022)

A race condition between the storage system and services database has the potential to revert edits made to patient information upon first ingestion of a study.

Moderate

FDAJun 23, 2022AR, CA, CO +40 more• DICOM Grid, Inc. d/b/a Ambra Health

Crome Implantable Cardioverter Defibrillator (Medtronic) – Reduced Shock Energy (2022)

There is the potential for reduced shock energy (~79% of programmed energy) during high-voltage (HV) therapy for Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds).

Moderate

FDAJun 22, 2022Nationwide• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

E-100 Generator (Intuitive Surgical) – Maintenance Performance Issue (2022)

Due to preventative maintenance (PM) not being performed on E-100 generators which is a bipolar electrosugical unit designed to be used with the da Vinci Xi and X systems.

Moderate

FDAJun 22, 2022Nationwide• Intuitive Surgical, Inc.