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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

Class I (Serious)

Most Recent

Dec 2025

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 1641–1660 of 2670 recalls

Docetaxel Injection (Dr. Reddy's) – Defective Container (2017)

Defective Container: Product complaints received of defect in the seal of the Docetaxel injection vials that the aluminum seal and/or stopper is removed when the cap is flipped off.

Class IIModerate

FDAJan 9, 2017Nationwide• Dr. Reddy's Laboratories, Inc.

Cappuccino Snack Mix (Dutch Valley) – Potential Contamination (2017)

Salmonella

As a result of an ingredient supplier recall, Dutch Valley is issuing a recall on Cappuccino Snack Mix due to the potential for it to be contaminated with Salmonella.

Class IHigh

FDAJan 4, 2017DE, FL, GA +19 more• Dutch Valley Food Distributors Inc.

Flucanozole Tablets 100mg (Dr. Reddy's) – Failed Dissolution (2016)

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Failed Dissolution Specifications; 18 month stability time point

Class IIModerate

FDADec 28, 2016Nationwide• Dr. Reddy's Laboratories, Inc.

Flucanozole Tablets 50mg (Dr. Reddy's) – Failed Dissolution (2016)

Failed Dissolution Specifications; 18 month stability time point

Class IIModerate

FDADec 28, 2016Nationwide• Dr. Reddy's Laboratories, Inc.

Flucanozole Tablets 200mg (Dr. Reddy's) – Failed Dissolution (2016)

Failed Dissolution Specifications; 18 month stability time point

Class IIModerate

FDADec 28, 2016Nationwide• Dr. Reddy's Laboratories, Inc.

Flucanozole Tablets 150mg (Dr. Reddy's) – Failed Dissolution (2016)

Failed Dissolution Specifications; 18 month stability time point

Class IIModerate

FDADec 28, 2016Nationwide• Dr. Reddy's Laboratories, Inc.

Furosemide Tablets (Roxane) – Thick Tablet Issue (2016)

Failed Tablet/Capsule Specifications: An unusually thick tablet was reported through a complaint.

Class IIModerate

FDADec 22, 2016Nationwide• Roxane Laboratories, Inc.

Azelastine Nasal Spray (Roxane) – Droplet Size Problem (2016)

Defective Delivery System: out of specification result for droplet size distribution at the d90 measurement testing during the 6 month time point..

Class IIILow

FDADec 14, 2016Nationwide• Roxane Laboratories, Inc.

2017 THOR MOTOR COACH OUTLAW Recall: STRUCTURE:BODY:DOOR:HINGE AND ATTACHMENTS

Thor Motor Coach (TMC) is recalling certain model year 2016-2017 Outlaw motorhomes, models 37BG, 37LS, 37RB, 38RE and 38RF, manufactured January 13, 2016, to December 8, 2016. The affected vehicles have rear cargo door hinges with welds that may be inadequate for securing the hinge pin to the hinge plate.

NHTSADec 13, 2016Nationwide• THOR MOTOR COACH

Tortilla Enchilada (Tortillas Tita) – Production Contamination (2016)

Undeclared Allergen

Tortillas Tita initiated a voluntary recall of all lots of their Corn Tortillas and Tortilla Enchilada produced between September 2016 and December 7, 2016, due to undeclared allergen Wheat.

Class IIModerate

FDADec 8, 2016MI, OH, VA• Tortillas Tita, LLC

Corn Tortillas (Tortillas Tita) – Production Contamination (2016)

Undeclared Allergen

Tortillas Tita initiated a voluntary recall of all lots of their Corn Tortillas and Tortilla Enchilada produced between September 2016 and December 7, 2016, due to undeclared allergen Wheat.

Class IIModerate

FDADec 8, 2016MI, OH, VA• Tortillas Tita, LLC

2017 THOR MOTOR COACH QUANTUM Recall: EXTERIOR LIGHTING

Thor Motor Coach (TMC) is recalling certain model year 2017 Quantum RQ29 motorhomes manufactured June 27, 2016, to September 29, 2016. The affected vehicles may be missing a mid-ship marker light. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Systems (FMVSS) number 108, "Lamps, Reflective Devices, and Associated Equipment."

NHTSADec 2, 2016Nationwide• THOR MOTOR COACH

Domperidone Capsules (Jeffreys Drug Store) – Unapproved Medication (2016)

Marketed without an approved NDA/ANDA for which safety and efficacy has not been established.

Class IHigh

FDANov 23, 2016PA• Jeffreys Drug Store

2014 THOR MOTOR COACH TUSCANY Recall: ELECTRICAL SYSTEM

Fire/Burn Risk

Thor Motor Coach (TMC) is recalling certain model year 2014-2016 Tuscany motorhomes, models 40DX, 40KQ, 40RX, 42GX, 42WX, 44MT, 45AT and 45LT, manufactured April 11, 2013, to October 12, 2015. In the affected vehicles, water may leak into the keyless entry module and cause an electrical short.

NHTSANov 17, 2016Nationwide• THOR MOTOR COACH

Techni-Care Surgical Scrub (Care-Tech Labs) – Labeling Issue (2016)

Labeling: Incorrect or Missing Lot and/or Exp Date - Product is missing or has illegible lot and expiry codes, as well as defective or cracked caps.

Class IIILow

FDANov 8, 2016Nationwide• Care-Tech Laboratories, Inc.

MERITOR FRONT DRIVE STEER AXLE Equipment Recall: STEERING

Meritor, Inc. (Meritor) is recalling certain MX810 Series front drive steer axles, part numbers MX23810DANC7-538 and MX23810DANC8-538, manufactured May 27, 2016, to August 16, 2016 and equipped with MX25K lower king-pins. These lower king-pins may not meet design specifications and, as a result, may fracture, possibly causing a wheel end separation.

NHTSANov 3, 2016Nationwide• MERITOR

Metformin Tablets (Ascend Labs) – Foreign Tablet Contamination (2016)

Presence of Foreign Tablets/Capsules; report of Amlodipine Tablets found in 1000 count bottles of Metformin Hydrochloride Tablets USP

Class IIModerate

FDANov 2, 2016AL, FL, GA +2 more• Ascend Laboratories LLC

Mountain Bike Shock Absorbers (Fox Factory) – Injury Risk (2016)

This recall involves all model year 2016 and some 2017 FLOAT X2 bicycle rear shock absorbers sold both individually and installed on YT, Giant, Pivot, Intense, Ibis, Scott, Trek, GT, Knolly, Norco, Rocky Mountain, Diamondback, Morpheus, Foes Racing, Orbea and Canyon full-suspension mountain bikes and frames. The solid black or black and gold FLOAT X2 shocks have an air sleeve construction. FLOAT X2 is printed on the external reservoir connected to the blue compression and red rebound adjusters that have X2 and RVS laser etched on them. Recalled shocks do not have a "250 psi max" label directly under the air fill boss on the outer sleeve of the shock. Recalled shocks and bike models can be identified at http://ridefox.com/recall.

CPSCNov 1, 2016Nationwide• Fox Factory, Watsonville, Calif.

2014 SPARTAN MOTORS TRANSIT BUS CHASSIS CAB Recall: ENGINE AND ENGINE COOLING:EXHAUST SYSTEM

Fire/Burn Risk

Spartan Motors USA (Spartan) is recalling certain model year 2011-2017 Transit Bus Chassis Cabs manufactured February 17, 2011, to October 19, 2016. The affected vehicles have an exhaust tube that may disconnect at a joint near the underside of the floor, potentially exposing the floor to high temperatures for prolonged time periods.

NHTSANov 1, 2016Nationwide• SPARTAN MOTORS

Phenazopyridine Hydrochloride 200mg (Nationwide Laboratories) – CGMP Manufacturing Risk (2016)

CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.

Class IIModerate

FDAOct 28, 2016Nationwide• Nationwide Laboratories, LLC