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Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan

Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan Recalls

All product recalls associated with Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan.

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Recall Summary

Total Recalls

1000

Past Year

620

Class I (Serious)

Most Recent

Dec 2025

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 21–40 of 10937 recalls

Olympus OER-Pro (Aizu Olympus) – Maintenance Warning (2025)

Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.

FDAOct 31, 2025Nationwide• Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan

Olympus OER-Mini (Aizu Olympus) – Maintenance Warning (2025)

Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.

FDAOct 31, 2025Nationwide• Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan

Olympus OER-Elite (Aizu Olympus) – Maintenance Warning (2025)

Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.

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FDAOct 31, 2025Nationwide• Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan

Ranger XP 1000 NorthStar (Polaris) – Vehicle Safety Concern (2025)

Fire/Burn Risk

This recall involves certain VINs of Polaris Model Year 2025-2026 Ranger XP 1000 NorthStar and Ranger Crew XP 1000 NorthStar ROVs. The recalled vehicles were sold in black, blue, bronze, brown, camouflage, gray, orange, red and white. The vehicles were sold in three and six-seat configurations and have "POLARIS" stamped on the front grille. The VIN is printed on the left rear frame (on the driver's side of the vehicle) under the cargo box.

CPSCOct 30, 2025Nationwide• Polaris Industries Inc., of Medina, Minnesota

Potassium Chloride Injection (Otsuka) - Incorrect Labeling (2025)

Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq

Class IHigh

FDAOct 29, 2025Nationwide• Otsuka ICU Medical LLC

Potassium Chloride Injection (Otsuka) - Incorrect Labeling (2025)

Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq

Class IHigh

FDAOct 29, 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

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

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).

FDAOct 24, 2025Nationwide• GE Medical Systems, LLC

LEACHOI Bed Rail (Mobility Source) – Entrapment Risk (2025)

This recall involves LEACHOI Bed Rails, ASIN B0BZVCG2R5. The bed rail comes in black/silver and weighs 7.72 pounds. The product measures 15.6 inches by 25.4 inches by 24 inches.

CPSCOct 23, 2025Nationwide• Mobility Source Medical Technology Co., Ltd, of China

Ice Cream Factory Graham Pieces – Foreign Material Risk (2025)

Foreign material fragments consisting of aluminum foil and packaging material were identified in brown sugar ingredient that may have been used in the products

Class IIModerate

FDAOct 23, 2025AL, AR, FL +26 more• Ice Cream Factory, LLC

CareLink Clinic (Medtronic) – Graph Data Inaccuracy (2025)

Software error causing incorrect data to be displayed on the 24-hour Sensor Glucose Overview Graph, any potential therapy decisions were made based on the incorrect data displayed on the 24-hour sensor glucose overview graph may lead to hypoglycemia or hyperglycemia.

FDAOct 21, 2025Nationwide• Medtronic MiniMed, Inc.

Opdualag Injection (Bristol-Myers Squibb) – Sterility Concern (2025)

Lack of Assurance of Sterility.

Class IIModerate

FDAOct 21, 2025Nationwide• Bristol-Myers Squibb Company