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SUN PHARMACEUTICAL INDUSTRIES INC

SUN PHARMACEUTICAL INDUSTRIES INC Recalls

All product recalls associated with SUN PHARMACEUTICAL INDUSTRIES INC.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 3841–3860 of 25002 recalls

Dofetilide Capsules (Sun Pharma) – Content Uniformity Issue (2023)

Out of Specification result observed in content uniformity testing

Class IIILow

FDAJul 18, 2023Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Proclaim DRG Pulse Generator (Abbott) – MRI Mode Malfunction (2023)

Firm has received complaints from patients who are unable to exit MRI (Magnetic Resonance Imaging) mode on their IPGs (Implantable Pulse Generators).

Moderate

FDAJul 18, 2023Nationwide• Abbott Medical

RayCare Software (RaySearch) – Allergy Warning Issue (2023)

An issue was found in Software RayCare 5A, 5B, 6A, including service packs, where an allergy warning against medication substance (drug ingredient) will not be displayed as expected under certain circumstances

1...191 192193194 195...1251

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High

FDAJul 17, 2023Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

Aquilex Fluid System (WOM) – Volume Display Limit (2023)

The display of inflow volume can reach its limit of 30,000 ml during long procdeure and the inflow volume display will freeze at the maximum value while the deficit will start counting backwards until 0 ml is reached and may result in fluid overload

High

FDAJul 17, 2023Nationwide• WOM World Of Medicine AG Alte Poststr. 11 Ludwigsstadt Germany

Outshine Strawberry Fruit Bars (Dreyer's) – Milk Allergen Alert (2023)

Undeclared Allergen

Undeclared allergen; milk.

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SUN PHARMACEUTICAL INDUSTRIES INC Recalls

Recall Summary

Dofetilide Capsules (Sun Pharma) – Content Uniformity Issue (2023)

Proclaim DRG Pulse Generator (Abbott) – MRI Mode Malfunction (2023)

RayCare Software (RaySearch) – Allergy Warning Issue (2023)

Aquilex Fluid System (WOM) – Volume Display Limit (2023)

Outshine Strawberry Fruit Bars (Dreyer's) – Milk Allergen Alert (2023)

Fentanyl Sodium Chloride Bag (Central Admixture) – Sterility Validation Issue (2023)

Phenylephrine 1000mcg/10mL Syringe (Central Admixture) – Sterility Concern (2023)

Phenylephrine 400mcg/10mL Sodium Chloride (Central Admixture) – Sterility Concern (2023)

Phenylephrine Sodium Chloride Syringe (Central Admixture) – Sterility Validation Issue (2023)

Fentanyl 10mcg/1mL Sodium Chloride (Central Admixture) – Sterility Concern (2023)

Fentanyl 100mcg/10mL Sodium Chloride (Central Admixture) – Sterility Concern (2023)

Fentanyl 2500mcg/50mL Syringe (Central Admixture) – Sterility Concern (2023)

Midazolam Dextrose Syringe (Central Admixture) – Sterility Validation Issue (2023)

Morphine Sodium Chloride Syringe (Central Admixture) – Sterility Validation Issue (2023)

Hydromorphone Sodium Chloride Syringe (Central Admixture) – Sterility Validation Issue (2023)

Morphine Sodium Chloride Syringe (Central Admixture) – Sterility Validation Issue (2023)

Fentanyl Dextrose Syringe (Central Admixture) – Sterility Validation Issue (2023)

Hydromorphone Dextrose Syringe (Central Admixture) – Sterility Validation Issue (2023)

Fentanyl Syringe (Central Admixture) – Sterility Validation Issue (2023)

Fentanyl Bag (Central Admixture) – Sterility Validation Issue (2023)