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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

726

Class I (Serious)

175

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 2301–2320 of 11124 recalls

Telmisartan Hydrochlorothiazide Tablets (Glenmark) – Packaging Issue (2022)

Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .

Class IIModerate

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

Naphcon A 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

Desmopressin Acetate Tablets (Glenmark) – Manufacturing Deviation (2022)

CGMP Deviations

1...114 115116117 118...557

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Class II

Moderate

FDAJun 29, 2022IN, TX• Glenmark Pharmaceuticals Inc., USA

Debrox Earwax Removal Aid (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

Telmisartan Hydrochlorothiazide Tablets (Glenmark) – Packaging Issue (2022)

Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .

Class IIModerate

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

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 IIModerate

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

Stryker 2.3mm Tapered Router (Stryker) – Potential Router Breakage (2022)

There is a potential for the core diameter to be undersized, which may lead to the router breaking. A break can lead to unintended metal fragments in the surgical site, resulting in the potential for surgical intervention or damage to critical neurological or vascular structures.

Moderate

FDAJun 24, 2022Nationwide• Stryker Instruments

Coda Pendant Light Fixtures – impact injury risk (2022)

The recalled Coda pendant is a clear or smoke glass suspended light fixture that provides general illumination and is available in two sizes, large (40" high and weighs 7 lbs.) and small (21" high and weighs 4 lbs.). The model/item number is on the light fixture packaging. The light uses an integrated LED light source. The recall involves the following model numbers: Item Number Description 700TDCDAPLCCS-LED930 Coda Large, Clear Glass 700TDCDAPLKCS-LED930 Coda Large, Smoke Glass 700TDCDAPSCCS-LED930 Coda Small, Clear Glass 700TDCDAPSKCS-LED930 Coda Small, Smoke Glass 365TDMISC4052 Custom spare part LED module with 20' cord 365TDCODALS-A Spare part LED module

Moderate

CPSCJun 23, 2022Nationwide• Guangzhou Xiongyi Precision Metalworking Co. Ltd., of China