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Daiichi Sankyo Pharma Development

Daiichi Sankyo Pharma Development Recalls

All product recalls associated with Daiichi Sankyo Pharma Development.

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Recall Summary

Total Recalls

1000

Past Year

590

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 7801–7820 of 10391 recalls

Benicar HCT Tablets (Daiichi Sankyo) – Temperature Storage Issue (2014)

Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping

Class IIModerate

FDAJul 12, 2014Nationwide• Daiichi Sankyo Pharma Development

Tribenzor Tablets (Daiichi Sankyo) – Temperature Storage Issue (2014)

Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping

Class IIModerate

FDAJul 12, 2014Nationwide• Daiichi Sankyo Pharma Development

Azor Tablets (Daiichi Sankyo) – Temperature Storage Issue (2014)

Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping

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Class IIModerate

FDAJul 12, 2014Nationwide• Daiichi Sankyo Pharma Development

Benicar HCT Tablets (Daiichi Sankyo) – Temperature Storage Issue (2014)

Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping.

Class IIModerate

FDAJul 12, 2014Nationwide• Daiichi Sankyo Pharma Development

Benicar Tablets (Daiichi Sankyo) – Temperature Storage Issue (2014)

Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping.

Class IIModerate

FDAJul 12, 2014Nationwide• Daiichi Sankyo Pharma Development

Benicar Tablets (Daiichi Sankyo) – Temperature Storage Issue (2014)

Temperature Abuse; various products were not stored at Controlled Room Temperature as per USP guidelines during shipping

Class IIModerate

FDAJul 12, 2014Nationwide• Daiichi Sankyo Pharma Development

Sodium Chloride Injection (Baxter) – Particulate Contamination (2014)

Presence of Particulate Matter: particulate matter identified as fibers and/or plastics.

Class IHigh

FDAJul 11, 2014Nationwide• Baxter Healthcare Corp.

Sodium Chloride Injection (Baxter) – Particulate Contamination (2014)

Presence of Particulate Matter: particulate matter identified as fibers and/or plastics.

Class IHigh

FDAJul 11, 2014Nationwide• Baxter Healthcare Corp.

Potassium Chloride Injection (Baxter) – Particulate Contamination (2014)

Presence of Particulate Matter: particulate matter identified as fibers and/or plastics

Class IHigh

FDAJul 11, 2014Nationwide• Baxter Healthcare Corp.

Cumberland Cheese (Sequatchie Cove) – E. Coli Contamination (2014)

Sample of cheese taken by FDA was found to contain generic E Coli.

Class IIModerate

FDAJul 7, 2014TN• Ledgendairy Cheeseworks, LLC DBA Sequatchie Cove Creamery

Single Stage Snow Thrower (All Power) – Fire Hazard (2014)

Fire/Burn Risk

This recall involves All Power brand single stage snow throwers. The snow throwers are black and yellow and have a red cap on the gas tank. They have a 20-inch wide snow clearing width and an 87cc, 4-cycle engine. The model number of the recalled snow throwers is SB044P which is printed on a yellow and black sticker located on the top of the unit with the phrase "20 Inch Clearing Width."

CPSCJul 2, 2014Nationwide• Suzhou Murray Machinery Manufacturing Co., Ltd. Jiangsu, China

2015 THOR MOTOR COACH VEGAS Recall: EQUIPMENT:RECREATIONAL VEHICLE/TRAILER

Thor Motor Coach (Thor) is recalling certain model year 2014-2015 Axis and Vegas motorhomes manufactured August 2, 2013, to June 18, 2014. Due to the use of an incorrect adhesive, the treads on the entry stairs into the vehicle may come loose.

NHTSAJul 1, 2014Nationwide• THOR MOTOR COACH

Ibuprofen Tablets 600mg (American Health) – Labeling Mix-Up (2014)

Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg, lot #142588 that contain blister cards filled with Ibuprofen tablets, 600mg drug product, were found to be mis-labeled with blister card print identifying the product as AHP Oxcarbazepine Tablets, 300mg, lot #142544

Class IHigh

FDAJul 1, 2014Nationwide• American Health Packaging