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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

1000

Class I (Serious)

143

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 3741–3760 of 37665 recalls

Sirolimus Tablets (Dr. Reddy's) – Impurity Specification Failure (2024)

Failed Impurities/Degradation Specifications

Class IIILow

FDAMay 1, 2024Nationwide• Dr. Reddy's Laboratories, Inc.

TabloCart (Outset Medical) – Cord Connector Defect (2024)

A cart with prefiltration drawer, an optional hemodialysis system accessory, has a cord with a female connector that has internal contact pins that may become damaged that could create localized heat, sparks, smoke, melting or charring (thermal event) of the female connector or the associated connector power entry module, which may lead to transient delay in treatment or blistering to the user.

High

FDAApr 30, 2024Nationwide• Outset Medical, Inc.

Agilis NxT Steerable Introducer (St. Jude) – Short Dilators (2024)

One lot of product has dilators that are too short and will not extend outside the introducer sheath.

1...186 187188189 190...1884

Page 188 of 1884Next

Moderate

FDAApr 30, 2024Nationwide• St. Jude Medical

Medline Iris Scissors (Medline) – Tip Protector Issue (2024)

There is the potential of the tip protector to fall off 4.5" sterile, curved, Iris Scissors

Low

FDAApr 30, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

Fentanyl Injection (Hikma) – Incorrect Barcode (2024)

Labeling: Wrong Barcode

Class IIILow

FDAApr 30, 2024Nationwide• Hikma Injectables USA Inc

FiberOptix IAB Catheter Kit (Arrow) – Health Consequence (2024)

Teleflex received reports indicating an infrequent condition that, when not identified and corrected promptly, could result in serious health consequences. The issue may manifest as: -failure of the intra-aortic balloon to completely inflate over its full length -damaged or broken central lumen in the segment contained within the balloon -helium loss or blood in the helium pathway.

High

FDAApr 29, 2024Nationwide• ARROW INTERNATIONAL Inc.

UltraFlex IAB Catheter Kit (Arrow) – Health Consequence (2024)

High

FDAApr 29, 2024Nationwide• ARROW INTERNATIONAL Inc.

Ultra 8 IAB Catheter Kit (Arrow) – Health Consequence (2024)

High

FDAApr 29, 2024Nationwide• ARROW INTERNATIONAL Inc.

Decompression Table (Pivotal Health) – Frame Part Issue (2024)

This product is being recalled due to potentially insufficient rework on a part (E7130-B) on the lumbar section of the frame on 6 distributed tables. There were 4 additional tables with the faulty E7130-B part that were manufactured, but had not been distributed yet.

Low

FDAApr 29, 2024CA, FL, GA +3 more• Pivotal Health Solutions, Inc.

Reading Truck RM-78 (Reading) – Taillight Position (2024)

Reading Truck Body LLC (Reading) is recalling certain 2022-2024 RM-78 11' and RM-78 14' vehicles. The taillight may be incorrectly positioned, exceeding the maximum allowed height. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."

Low

NHTSAApr 29, 2024Nationwide• READING TRUCK EQUIPMENT

Phenylephrine Injection (Hikma) – Label Mix-up (2024)

Labeling: Label mix-up - ephedrine syringes mislabeled as phenylephrine.

Class IHigh

FDAApr 29, 2024CO, GA, PA +2 more• Hikma Injectables USA Inc

H-E-B Creamy Creations Chocolate Ice Cream (H-E-B) – Metal Contamination (2024)

Potential metal contamination

Class IIModerate

FDAApr 27, 2024TX• H-E-B San Antonio Retail Support Center (SARSC)

H-E-B Creamy Creations Homemade Ice Cream (H-E-B) – Metal Contamination (2024)

Potential metal contamination

Class IIModerate

FDAApr 27, 2024TX• H-E-B San Antonio Retail Support Center (SARSC)

H-E-B Creamy Creations Lime/Orange Ice Cream (H-E-B) – Metal Contamination (2024)

Potential metal contamination

Class IIModerate

FDAApr 27, 2024TX• H-E-B San Antonio Retail Support Center (SARSC)

O-arm O2 Imaging System (Medtronic) – Electrical Component (2024)

Potential for an electrical component of the O-arm" O2 Imaging System to intermittently shut off,failure can cause the potential for surgical delay, additional imaging, cancellation and rescheduling of surgery, or completion of surgery without the benefit of image guidance.

High

FDAApr 26, 2024Nationwide• Medtronic Navigation, Inc.-Littleton

Acumatch Bipolar Liner (Exactech) – Packaging Layer (2024)

The AcuMatch L-Series 22mm Inner Diameter Bipolar Hip Liner lots were packaged without the specified ethylene vinyl alcohol (EVOH) layer. Between 2004 and August 2021, our packaging process utilized two different types of packaging materials: 1) Low Density Polyethylene (LDPE), Nylon, and EVOH, or 2) LDPE and Nylon without EVOH.

Low

FDAApr 26, 2024IN, PR• Exactech, Inc.

CDC H5 Influenza Subtyping Kit – Amplification Failure (2024)

The H5b component may fail to amplify, resulting in an inconclusive result.

Moderate

FDAApr 26, 2024Nationwide• Centers For Disease Control and Prevention

Tramadol Tablets (Rubicon) – Foreign Tablet Presence (2024)

Presence of Foreign Tablets: Pharmacist reported a tablet of baclofen in a bottle of 1000-count tramadol

Class IIModerate

FDAApr 26, 2024Nationwide• Rubicon Research Private Limited

StarDrive Screwdriver (Synthes) – Tip Engagement (2024)

Laceration Risk

Stardrive Screwdrivers manufactured without a 5-degree relief cut around the tip and will not engage with their respective 1.3mm and 1.5mm screws, may result in surgical delay

Low

FDAApr 25, 2024Nationwide• Synthes (USA) Products LLC

Peltor X4 Series Earmuffs (3M) – Noise Exposure Risk (2024)

This recall involves 3M's Peltor X4 series earmuffs designed for noise reduction in industrial and occupational applications. The recalled earmuffs are black with green or orange accents and are over-the-head, behind-the-head, hard hat-attached, or full brim hard hat-attached. 3M PELTOR is stamped on the outside of the earcups. Only earmuffs manufactured from March 2020 through September 2022 are included in this recall. The date of manufacture in MM/YYYY format appears on the outside of the earmuff's earcups.

Low

CPSCApr 25, 2024Nationwide• 3M Company, of Saint Paul, Minnesota