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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 1541–1560 of 21319 recalls

Diltiazem Hydrochloride Capsules 90mg (Glenmark) – Impurity Risk (2024)

cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.

Class IIModerate

FDANov 1, 2024Nationwide• Glenmark Pharmaceuticals Inc., USA

Diltiazem Hydrochloride Capsules 60mg (Glenmark) – Impurity Risk (2024)

cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.

Class IIModerate

FDANov 1, 2024Nationwide• Glenmark Pharmaceuticals Inc., USA

Diltiazem Hydrochloride Capsules 90mg (Glenmark) – Impurity Risk (2024)

cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.

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Class IIModerate

FDANov 1, 2024Nationwide• Glenmark Pharmaceuticals Inc., USA

BACTEC 9240 System (Becton Dickinson) – credential access risk (2024)

BD confirmed that product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.

Low

FDAOct 31, 2024Nationwide• Becton Dickinson & Co.

BD Synapsys Informatics Solution (Becton Dickinson) – credential access risk (2024)

Low

FDAOct 31, 2024Nationwide• Becton Dickinson & Co.

BD COR MX Instrument (Becton Dickinson) – credential access risk (2024)

Low

FDAOct 31, 2024Nationwide• Becton Dickinson & Co.

EVIS EXERA III Videoscope (Olympus) – disinfection compatibility issue (2024)

High-level disinfection ("HLD") with Acecide-C disinfectant in the Olympus OER-Pro Automated Endoscope Reprocessor ("AER") has been removed as a compatible reprocessing method from the Instructions for Use when reprocessing the GIF-1THI90 EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE ( GIF-1TH190 ).

Low

FDAOct 31, 2024Nationwide• Olympus Corporation of the Americas

BD EpiCenter Data Management System (Becton Dickinson) – credential access risk (2024)

Low

FDAOct 31, 2024Nationwide• Becton Dickinson & Co.

BD BACTEC FX Instrument (Becton Dickinson) – credential access risk (2024)

Low

FDAOct 31, 2024Nationwide• Becton Dickinson & Co.

BD COR PX Instrument (Becton Dickinson) – credential access risk (2024)

Low

FDAOct 31, 2024Nationwide• Becton Dickinson & Co.

Hybrid Recon Software (Hermes Medical) – reconstruction alignment risk (2024)

Due a potential software/configuration issue that may result is incorrect alignment during reconstructing a SPECT/CT study.

Moderate

FDAOct 31, 2024CA, CT, FL +12 more• Hermes Medical Solutions AB Strandbergsgatan 16 Stockholm Sweden

BD MAX System (Becton Dickinson) – credential access risk (2024)

Low

FDAOct 31, 2024Nationwide• Becton Dickinson & Co.

Cook Medical Hemospray Hemostat (Wilson-Cook) – activation knob defect (2024)

Specific lots of product have been manufactured with nonconforming raw materials resulting in the red activation knob cracking or breaking at the activation knob internal threading while the device is activated.

High

FDAOct 31, 2024Nationwide• Wilson-Cook Medical Inc.