Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
SUN PHARMACEUTICAL INDUSTRIES INC

SUN PHARMACEUTICAL INDUSTRIES INC Recalls

All product recalls associated with SUN PHARMACEUTICAL INDUSTRIES INC.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

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 2801–2820 of 21320 recalls

Cinacalcet Tablets 60mg (Sun Pharmaceutical) – Microbial Contamination (2024)

CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.

Class IIModerate

FDAJan 18, 2024Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Mesalamine Delayed-Release Tablets (Sun Pharmaceutical) – Microbial Contamination (2024)

CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.

Class IIModerate

FDAJan 18, 2024Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Fexofenadine Hydrochloride Tablets 180mg (Sun Pharmaceutical) – Microbial Contamination (2024)

CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.

1...139 140141142 143...1066

Page 141 of 1066Next

Class IIModerate

FDAJan 18, 2024Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

InstaClear Lens Cleaner (Olympus) – Instructions Variation (2024)

Japanese IFU version had slightly different language and illustrations from the English IFU, which could contribute to the tip and plate falling off. In order to maintain consistency globally, the Japanese IFU will be updated to reflect the instructions in the English IFU

Low

FDAJan 16, 2024Nationwide• Olympus Corporation of the Americas

MIC Gastric-Jejunal Feeding Tube (Avanos) – Syringe Recall (2024)

MIC* Gastric - Jejunal Feeding Tube Kits contain a sterile pre-filled syringe subsequently recalled by Nurse Assist.

High

FDAJan 16, 2024Nationwide• Avanos Medical, Inc.

HLS Set Advanced (Maquet) – Sterile Barrier Compromise (2024)

The Emergency Priming Line, a component of the HLS Set, may have a compromised sterile barrier due to nonconformities at the bag seal. This issue may result in inflammation, sepsis, or infection.

High

FDAJan 16, 2024Nationwide• Maquet Medical Systems USA

HLS Set Advanced (Maquet) – Sterile Barrier Compromise (2024)

The Emergency Priming Line, a component of the HLS Set, may have a compromised sterile barrier due to nonconformities at the bag seal. This issue may result in inflammation, sepsis, or infection.

High

FDAJan 16, 2024Nationwide• Maquet Medical Systems USA

Water Filter MAJ-2318 (Olympus) – Incorrect Assembly (2024)

Water filter may have been assembled incorrectly, resulting in unfiltered tap water being used for reprocessing. This may expose a patient to a potentially contaminated device, presenting a risk of infection or sepsis.

High

FDAJan 16, 2024Nationwide• Olympus Corporation of the Americas

IV Start Kit (Medical Action) – Saline Syringe Recall (2024)

The kits contain saline flush syringes which were recalled by the supplier.

High

FDAJan 15, 2024Nationwide• Medical Action Industries, Inc.

Phenoxybenzamine Hydrochloride Capsules (Amneal) – Impurity Specification (2024)

Failed Impurities/Degradation Specifications: Out of specification for unknown impurity.

Class IIModerate

FDAJan 15, 2024Nationwide• Amneal Pharmaceuticals of New York, LLC

Directional Laser Probe (D.O.R.C.) – Fiber Extension Problem (2024)

When using those products you may experience difficulties to extend or retract the laser fiber, and in some occasions may also have difficulties to direct the laser fiber tip precisely.

Moderate

FDAJan 15, 2024Nationwide• D.O.R.C. Dutch Opthalmic Research Center Intl B.V. Scheijdelveweg 2 Zuidland Netherlands

Budesonide Tablets (Golden State Medical) – Failed Dissolution (2024)

Failed Dissolution Specifications

Class IIModerate

FDAJan 12, 2024IL• Golden State Medical Supply Inc.

Vasopressin Sodium Chloride (IntegraDose) – Subpotent Drug (2024)

Subpotent Drug

Class IIModerate

FDAJan 12, 2024MN• IntegraDose Compounding Services LLC

Colonoscope PCF-H180AL (Olympus) – Adhesive Deficiency (2024)

Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration, fluctuation in temperature or severe shock loads.

Moderate

FDAJan 11, 2024Nationwide• Olympus Corporation of the Americas