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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)

145

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 241–260 of 37661 recalls

Lisdexamfetamine 70mg Capsules (Sun) - Dissolution Failure (2025)

Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH) for Lisdexamfetamine dimesylate capsules.

Class IIModerate

FDAOct 28, 2025Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Lisdexamfetamine 10mg Capsules (Sun) - Dissolution Failure (2025)

Class IIModerate

FDAOct 28, 2025Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Lisdexamfetamine 40mg Capsules (Sun) - Dissolution Failure (2025)

1...11 121314 15...1884

Page 13 of 1884Next

Class IIModerate

FDAOct 28, 2025Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Lisdexamfetamine 60mg Capsules (Sun) - Dissolution Failure (2025)

Class IIModerate

FDAOct 28, 2025Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Azurion R3.0 (Philips) – SSD Spacer Omission (2025)

Between July 2024 and June 2025, Philips Azurion R3.0 systems with a FlexArm stand were shipped without the Source-to-Skin Distance (SSD) Spacer. The SSD spacer is necessary to meet the FDA minimum source-skin distance requirement of 38 cm for standard fluoroscopy applications.

Moderate

FDAOct 27, 2025Nationwide• Philips North America

Tesla Cybertruck (Tesla) – Exterior Lighting Accessory Problem (2024)

Tesla, Inc. (Tesla) is recalling certain 2024 Cybertruck vehicles equipped with a service-installed off-road light bar accessory. An incorrect surface primer may have been used to attach the lightbar to the windshield, causing the light bar to loosen and detach.

High

NHTSAOct 27, 2025Nationwide• TESLA

Vegetable Carton Label (Pacific International) – Salmonella Risk (2025)

Salmonella

Potential contamination with Salmonella.

Class IHigh

FDAOct 27, 2025AZ, CA, FL +5 more• Pacific International Marketing

Vegetable Carton Label (Pacific International) – Salmonella Risk (2025)

Salmonella

Potential contamination with Salmonella.

Class IHigh

FDAOct 27, 2025AZ, CA, FL +5 more• Pacific International Marketing

Fresh Herbs (Pacific International) – Salmonella Risk (2025)

Salmonella

Potential contamination with Salmonella.

Class IHigh

FDAOct 27, 2025AZ, CA, FL +5 more• Pacific International Marketing

Sodium Chloride Injection (Otsuka) - Sterility Risk (2025)

Lack of Assurance of Sterility: Potential for flexible container leaks.

Class IIModerate

FDAOct 27, 2025Nationwide• Otsuka ICU Medical LLC

Vegetable Carton Label (Pacific International) – Salmonella Risk (2025)

Salmonella

Potential contamination with Salmonella.

Class IHigh

FDAOct 27, 2025AZ, CA, FL +5 more• Pacific International Marketing

Farmhouse White Cheese (Peterson Company) – E. coli Risk (2025)

E. coli

Item #29608 Farmhouse White is recalled due to E. coli O103:H2.

Class IHigh

FDAOct 25, 2025CO, ID, IN +2 more• Peterson Company Inc

Whatcom Blue Cheese (Peterson Company) – E. coli Risk (2025)

E. coli

Item #28855 Whatcom Blue is recalled due to E. coli O103:H2

Class IHigh

FDAOct 25, 2025CO, ID, IN +2 more• Peterson Company Inc

Forest River XLR Toyhauler (Forest River) – Plumbing Mounting Issue (2021)

Forest River, Inc. (Forest River) is recalling certain 2021 XLR Toy Hauler travel trailers. The mounting brackets may be improperly located or secured, allowing the fresh water tank to detach when full.

High

NHTSAOct 24, 2025Nationwide• FOREST RIVER

Twin Sisters Peppercorn Cheese (Twin Sisters Creamery) – E. coli Risk (2025)

E. coli

Raw milk Peppercorn cheese is recalled due to E.coli O26:H11

Class IHigh

FDAOct 24, 2025IN, OR, WA• Twin Sisters Creamery, LLC

Twin Sisters Mustard Seed Cheese (Twin Sisters Creamery) – E. coli Contamination (2025)

E. coli

Raw milk Mustard Seed cheese is recalled due to E. coli O103:H2 and E. coli O74:H25.

Class IHigh

FDAOct 24, 2025IN, OR, WA• Twin Sisters Creamery, LLC

Twin Sisters Whatcom Blue Cheese (Twin Sisters Creamery) – E. coli Risk (2025)

E. coli

Raw milk Whatcom Blue cheese is recalled due to E. coli O103:H2.

Class IHigh

FDAOct 24, 2025IN, OR, WA• Twin Sisters Creamery, LLC

Twin Sisters Farmhouse Cheese (Twin Sisters Creamery) – E. coli Contamination (2025)

E. coli

Raw milk Farmhouse cheeses are recalled due to E. coli O103:H2 and E. coli O74:H25.

Class IHigh

FDAOct 24, 2025IN, OR, WA• Twin Sisters Creamery, LLC

Senographe Pristina (GE Medical) – X-Ray Warning Label Missing (2025)

Some Senographe Pristina systems either have a missing or an incorrect X-Ray Warning label, which is a nonconformance to FDA Regulation 21 CFR 1020.30(j).

Moderate

FDAOct 24, 2025Nationwide• GE Medical Systems, LLC

My Bladder Supplement (Water Pure) – E. coli Contamination (2025)

E. coli

Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303

Class IIModerate

FDAOct 24, 2025Nationwide• Water Pure, Inc.