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Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd. Recalls

All product recalls associated with Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd..

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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 2601–2620 of 25002 recalls

Abilify 5mg Tablets (Otsuka) – Product Contamination (2024)

Cross Contamination with Other Products

Class IIILow

FDAApr 9, 2024Nationwide• Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Abilify 10mg Tablets (Otsuka) – Product Contamination (2024)

Cross Contamination with Other Products

Class IIILow

FDAApr 9, 2024Nationwide• Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Pottery Barn Travel Trailer (Airstream) – Incorrect Axle Label (2024)

Airstream, Inc. (Airstream) is recalling certain 2024 Pottery Barn travel trailers. The rear axle weight on the Federal Certification label is incorrect. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 110, "Tire Selection and Rims."

1...129 130131132 133...1251

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Low

NHTSAApr 9, 2024Nationwide• AIRSTREAM

Samaritan PAD Defibrillator (HeartSine) – Voice Prompt Malfunction (2024)

Automated external defibrillators have a manufacturing issue that could prevent the device from delivering instructional voice prompts to the user during use of the device. Visual instructional icons will still be present, but this issue could potentially lead to no therapy or a delay in therapy.

Moderate

FDAApr 8, 2024Nationwide• HeartSine Technologies Ltd 207 Airport Road West Belfast United Kingdom

Twin Tube Sample Line (Vyaire) – Nozzle Separation Risk (2024)

Potential of the nozzle separating during patient use.

Low

FDAApr 8, 2024Nationwide• Vyaire Medical, Inc. Leibnizstr. 7 Hochberg Germany

Ready Meals Teriyaki Salmon (Taylor Farms) – Mislabeled Product (2024)

The firm is recalling 6 packages of Teriyaki Salmon that was mislabeled as Teriyaki Chicken.

Class IIModerate

FDAApr 8, 2024IN• Taylor Farms Southwest, Inc

ZirCAD Ceramic Block (Ivoclar) – Sintering Crack Risk (2024)

Defective blocks may show cracks after sintering If cracks are unnoticed, restorations may fracture in the patient's mouth and require restoration

Moderate

FDAApr 5, 2024Nationwide• IVOCLAR VIVADENT AG BEDERSRASSE LIECHTSTEIN Germany

3 mL Luer Lock Syringe (Wolf Medical) – Configuration Mismatch (2024)

Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).

Low

FDAApr 5, 2024Nationwide• Jiangsu Shenli Medical Production Co., Ltd. No.

3 mL Luer Lock Syringe (GMAX) – Configuration Mismatch (2024)

Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).

Low

FDAApr 5, 2024Nationwide• Jiangsu Shenli Medical Production Co., Ltd. No.

30 mL Luer Slip Syringe (Medline) – Configuration Mismatch (2024)

Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).

Low

FDAApr 5, 2024Nationwide• Jiangsu Shenli Medical Production Co., Ltd. No.

DBX Vehicle (Aston Martin) – Battery Fuse Box Wiring (2024)

Aston Martin The Americas (Aston Martin) is recalling certain 2021-2024 DBX vehicles. Electrical cables in the battery fuse box may be loose, which can result in an engine stall, or a loss of headlights and/or power steering.

High

NHTSAApr 5, 2024Nationwide• ASTON MARTIN

Evidence MultiSTAT Analyzer (Randox) – Foam Gasket Malfunction (2024)

Foam gasket on the Evidence MultiSTAT chip heater assembly may not perform as expected. Foam that is not functioning as expected may cause light to leak into the Charged Coupled Device (CCD) Camera during imaging. This will affect the testing and may delay in reporting results.

Low

FDAApr 5, 2024Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

WOLF-PAK 1 mL Disposable Syringe (Wolf Medical) – Configuration Mismatch (2024)

Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).

Low

FDAApr 5, 2024Nationwide• Jiangsu Shenli Medical Production Co., Ltd. No.

100 mL Luer Lock Syringe (Medigrative) – Configuration Mismatch (2024)

Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).

Low

FDAApr 5, 2024Nationwide• Jiangsu Shenli Medical Production Co., Ltd. No.

Tide Pods (Procter & Gamble) – Defective Packaging (2024)

This recall involves certain lot codes of Tide Pods, Gain Flings, Ace Pods, and Ariel Pods liquid laundry detergent packets packaged in flexible film bags that were manufactured between September 2023 and February 2024. Recalled products range from bags with 12 to 39 laundry detergent packets and include the following: Gain Flings Original Tide Simply Pods Plus Oxi Boost Gain Flings Moonlight Breeze Scent Tide Pods Clean Breeze Scent Gain Flings Blissful Breeze Scent Tide Pods Free & Gentle Gain Flings Spring Daydream Scent Tide Pods Oxi Gain Flings Plus Ultra Oxi Tide Pods Ultra Oxi Gain Flings Plus Odor Defense Ace Pods Clean Breeze Tide Pods Original Ace Pods Spring Meadow Tide Pods Spring Meadow Scent Ariel Pods Alpine Breeze Tide Pods Light

Very High

CPSCApr 5, 2024Nationwide• The Procter & Gamble Company, of Cincinnati, Ohio

Tejocote Root Products (Global Mix) – Dangerous Ingredient (2024)

Product contains Yellow Oleander

Class IHigh

FDAApr 5, 2024AL, AK, CA +39 more• GLOBAL MIX INC.

IntelliSpace Cardiovascular Software (Philips) – Data Export Issue (2024)

Study data is not able to be archived, copied, or exported with the cardiovascular software version.

Low

FDAApr 4, 2024Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

Urinalysis Test Strips (Macherey Nagel) – Missing Test Pad (2024)

The reason for the recall is one of the test pads, for the parameter leukocytes, was missing on some of the test strips. The issue was identified by a consumer by way of a Henry Schein Inc. (HSI) customer complaint. This problem can potentially result in the possibility that the parameter leucocytes (a non-specific marker for urinary track infections and an indicator for inflammatory renal processes) is interpreted instrumentally as a false negative. The following HSI item number and lot number were affected: Urispec 11-Way, #102-2285, LOT 65402.

Low

FDAApr 4, 2024Nationwide• Macherey Nagel Gmbh & Co. Kg Valencienner Str. 11 Duren Germany

Scopis ENT Software (Stryker) – Visual Feedback Misalignment (2024)

Unreleased software was installed on customer systems resulting in the visual feedback on the screen to show the points to be off from the physical reference point of the pointer or suction.

Low

FDAApr 4, 2024Nationwide• Stryker Leibinger GmbH & Co. KG Botzinger Str. 41 Freiburg Im Breisgau Germany

Mainstays Electric Mini Choppers – Laceration Risk (2024)

Laceration Risk

This recall involves Mainstays Electric Mini Choppers with model number MS14100094536S1. The choppers are rechargeable and cordless, and have a green lid, white body, and clear plastic bowl. They have one blade attachment, which consists of three curved blades on one white plastic spindle. Model number MS14100094536S1 is on the label attached to the bottom of the clear plastic bowl.

High

CPSCApr 4, 2024Nationwide• Shuangma Plastic Manufacturing Inc., of China