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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

566

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 3601–3620 of 7756 recalls

Ranitidine Tablets 150mg (Dr. Reddy's) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDAOct 1, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Ranitidine Capsules 300mg (Dr. Reddy's) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDAOct 1, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Ranitidine Tablets 150mg (Dr. Reddy's) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class II

1...179 180181182 183...388

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Moderate

FDAOct 1, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Ranitidine Tablets 150mg (Dr. Reddy's) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDAOct 1, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Ranitidine Capsules 150mg (Dr. Reddy's) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDAOct 1, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Ranitidine Tablets 150mg (Dr. Reddy's) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDAOct 1, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Testosterone Cypionate Injection (New Vitalis) – Sterility Issue (2019)

Lack of sterility assurance.

Class IIModerate

FDAOct 1, 2019Nationwide• New Vitalis Pharmacy LLC dba New Vitalis Pharmacy

Ranitidine Tablets 75mg (Dr. Reddy's) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDAOct 1, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Ranitidine Tablets 150mg (Dr. Reddy's) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDAOct 1, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Ranitidine Tablets 150mg (Dr. Reddy's) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDAOct 1, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Ranitidine Tablets 150mg (GeriCare) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDAOct 1, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Ranitidine Tablets 75mg (Dr. Reddy's) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDAOct 1, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Ranitidine Tablets 150mg (Dr. Reddy's) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDAOct 1, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Ranitidine Tablets (Dr. Reddy's) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDAOct 1, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Ranitidine Tablets 150mg (Dr. Reddy's) – NDMA Impurity (2019)

CGMP Deviations: Presence of NDMA impurity detected in product.

Class IIModerate

FDAOct 1, 2019Nationwide• Dr. Reddy's Laboratories, Inc.

Testosterone Cypionate Injection (Arbor) – label mix-up (2019)

Labeling:Label Mix-up: Shipper Carton labelled Testosterone Cypionate Injection, USP, 200mg/mL, 1 ml single-dose vials, found to contain shelf cartons labelled as Testosterone Cypionate Injection USP, 200mg/mL, 10 ml multi-dose vials which contain Testosterone Cypionate Injection USP, 200mg/mL,1mL single-does vials

Class IIILow

FDASep 27, 2019Nationwide• Arbor Pharmaceuticals Inc.

CELLECT Cell Synergy (Cellect Products) – Heavy Metal Risk (2019)

Product contains unsafe levels of Arsenic and Lead

Class IIModerate

FDASep 27, 2019Nationwide• Images Unlimited Products, dba Cellect Products

Brainlab AG Olof-palme-str. 9 Munich Germany: Patient Data Manager, Model/Catalogue Numbers: 25100-0...

The Brainlab Patient Data Manager software (PDM) in combination with the Brainlab iPlan CMF/Cranial/ENT/Spine software 2.1.1, 2.2.0, 2.2.1, 2.3.0, 2.3.1, 2.4.0, 2.5.0, 2.5.1 (if used in combination with iPlan CMF/Cranial/ENT/Spine 3.0.5, 3.0.6) that may lead to shifts applied to segmentation objects in iPlan being not reflected when exported into DICOM under specific circumstances.

FDASep 25, 2019Nationwide• Brainlab AG Olof-palme-str. 9 Munich Germany

Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.: 4Fr x 20cm Single Lumen CT Midline Basic Tray, Product C...

Potential that 3Fr size catheter placed in the catheter tray instead of 4Fr for the 4Fr x 20cm Single Lumen CT Midline Basic Tray.

FDASep 24, 2019IN, TN• Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.

Randox Laboratories, Limited Ardmore; 55 The Diamond Road Crumlin United Kingdom: RANDOX NEFA (Non-Esterified Fatty Acids) FA115 Lot 485343...

Non-Esterified Fatty Acids (NEFA) FA115 batch 485343 is not meeting the performance claims and should not be used in any further testing.

FDASep 23, 2019WV• Randox Laboratories, Limited Ardmore; 55 The Diamond Road Crumlin United Kingdom