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Dr. Reddy's Laboratories, Inc.

Dr. Reddy's Laboratories, Inc. Recalls

All product recalls associated with Dr. Reddy's Laboratories, Inc..

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Recall Summary

Total Recalls

1000

Past Year

567

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 2341–2360 of 7756 recalls

Fexofenadine Pseudoephedrine Tablets (Dr. Reddy's) – dissolution failure (2021)

Failed dissolution specifications

Class IIILow

FDANov 12, 2021Nationwide• Dr. Reddy's Laboratories, Inc.

Allergy Relief D Tablets (Dr. Reddy's) – dissolution failure (2021)

Failed dissolution specifications

Class IIILow

FDANov 12, 2021Nationwide• Dr. Reddy's Laboratories, Inc.

Allergy & Congestion Tablets (Dr. Reddy's) – dissolution failure (2021)

Failed dissolution specifications

Class IIILow

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Page 118 of 388Next

FDA

Nov 12, 2021

Nationwide

• Dr. Reddy's Laboratories, Inc.

Antihistamine Decongestant (Dr. Reddy's) – Dissolution Failure (2021)

Failed dissolution specifications

Class IIILow

FDANov 12, 2021Nationwide• Dr. Reddy's Laboratories, Inc.

Allergy Relief D (Dr. Reddy's) – Dissolution Failure (2021)

Failed dissolution specifications

Class IIILow

FDANov 12, 2021Nationwide• Dr. Reddy's Laboratories, Inc.

Fexofenadine Pseudoephedrine Tablets (Dr. Reddy's) – dissolution failure (2021)

Failed dissolution specifications

Class IIILow

FDANov 12, 2021Nationwide• Dr. Reddy's Laboratories, Inc.

Allergy Relief D Tablets (Dr. Reddy's) – dissolution failure (2021)

Failed dissolution specifications

Class IIILow

FDANov 12, 2021Nationwide• Dr. Reddy's Laboratories, Inc.

Beckman Coulter Inc.: SYNCHRON Systems Cholesterol (CHOL) Reagent, REF: 467825

Cholesterol Reagent may fail with Out of Calibration Range Low (OCR Low) and/or Back to Back (B/B) errors. Low quality control recovery failures may be observed after passing calibration. Brown particulates in compartment C of the reagent cartridge may be observed. Continued use may lead to, 1) failed QC and/or calibrations, 2) Erroneous low Cholesterol patient results.

FDANov 10, 2021Nationwide• Beckman Coulter Inc.

Boston Scientific Corporation: Boston Scientific ROTAPRO, Rotational Atherectomy System ...

Manufacturing instructions did not include the directions to not retest the pneumatic kit component of the ROTAPRO console upon failure, an internal nonconformity.

FDANov 8, 2021Nationwide• Boston Scientific Corporation

Cefixime Capsules (Ascend) – Failed Impurities (2021)

Failed Impurities/Degradation Specifications

Class IIModerate

FDANov 3, 2021Nationwide• Ascend Laboratories LLC

Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland: RANDOX CHOL-cholesterol (total) test system intended to m...

When calibrating using the standard provided in the kit, the change in absorbance is lower than expected generating internal quality control results high outside range

FDANov 1, 2021Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Stradis Medical, LLC dba Stradis Healthcare: Custom Assemblies, Inc., Single Spike Tumescent Set w/o C...

This recall has been initiated to address bulk packed, non-sterile Intravascular Administration Sets that were erroneously distributed to fill orders for the sterile version of the same Intravascular Administration Set.

FDAOct 28, 2021CO, CT, MA +7 more• Stradis Medical, LLC dba Stradis Healthcare

Boston Scientific Corporation: HURRICANE RX DILATION BALLOON 4MM 2CM-for endoscopic dila...

Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure

FDAOct 21, 2021Nationwide• Boston Scientific Corporation

Instrumentation Laboratory: HemosIL ReadiPlasTin (20 mL), Part number 0020301400. An...

The firm has received customer reports of performance issues with the affected lot, including increased imprecision, out of range quality controls, and prolonged sample results. If quality controls are not performed or do not pass for each vial of reagent, there is a potential risk of reporting an erroneous result.

FDAOct 13, 2021Nationwide• Instrumentation Laboratory