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
/
FUJIFILM Healthcare Americas Corporation

FUJIFILM Healthcare Americas Corporation Recalls

All product recalls associated with FUJIFILM Healthcare Americas Corporation.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

896

Class I (Serious)

125

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 1561–1580 of 17592 recalls

FDR Visionary Suite (Fujifilm) – tube support risk (2024)

Bolts on the CH-200 tube may rupture due to fatigue failure, causing the tube support to fall, could result in patient injury

Moderate

FDAApr 11, 2024Nationwide• FUJIFILM Healthcare Americas Corporation

Dutchmen Aspen Trail Loft (Dutchmen) – suspension problem (2024)

Keystone RV Company7(Keystone) is recalling certain 2024 Keystone Retreat, Residence 40CLDL, Residence 401CLDL, Dutchmen Aspen Trail 421LOFT, and Crossroads Hampton 390PVL trailers. The equalizer may provide inadequate clearance, allowing the axle to contact the frame.

High

NHTSAApr 11, 2024Nationwide• DUTCHMEN

Quilts and Shams (Red Land Cotton) – Laceration Risk (2024)

Laceration Risk

This recall involves Red Land Cotton quilts and quilted shams. The Classic quilts come in white, natural, ticking stripe, blue, or gray, in all sizes: twin, full/queen, and king/California king sizes. The Classic quilted euro shams come in white, natural and ticking stripe. King and Standard shams are white, natural, blue, gray and ticking stripe. Baby quilts come in white, natural and charcoal ticking print.

1...77 787980 81...880

Page 79 of 880Next

High

CPSCApr 11, 2024Nationwide• Red Land Cotton, Moulton, Alabama

RC4 Junior Ski Boots (Fischer Sports) – Fall Hazard (2024)

This recall involves RC4 50, RC4 60, and RC4 65 Junior Ski Boots in sizes 21.5 to 27.5. The RC4 50 and RC4 60 were sold in Rhino Grey and Snow colors. The RC4 65 was sold in yellow. "Fischer" is printed on the lower shell on each boot, and the specific model and name is printed on the outside of the upper cuff, between the two top buckles. The size of the boot is stamped on the sole.

High

CPSCApr 11, 2024Nationwide• Fischer Sports US, of Auburn, New Hampshire

Noblus AC Adapter (Fujifilm) – power socket overheat (2024)

AC adapters of Noblus can heat up, and cause smoke in the worst case, when an excessive mechanical stress is applied to the socket for power cable (frequent insertion/removal of the power cable).

Moderate

FDAApr 11, 2024Nationwide• FUJIFILM Healthcare Americas Corporation

Leica HistoCore PEGASUS Processor (Leica) – reagent level issue (2024)

Poorly processed and/or damaged biopsy tissue specimens on the device resulting from reagent levels exceeding the maximum fill level marks on reagent bottles or in the paraffin tanks.

Low

FDAApr 10, 2024Nationwide• LEICA BIOSYSTEMS NUSSLOCH GMBH Heidelberger Str. 17-19 Nussloch Germany

CRITIKON ONE-CUF Blood Pressure Cuffs (GE Healthcare) – Inaccurate Measurements (2024)

Use of the blood pressure cuffs could result in inaccurate non-invasive blood pressure measurements.

Low

FDAApr 9, 2024Nationwide• GE Medical Systems Information Technologies Inc

Abilify 15mg Tablets (Otsuka) – Product Contamination (2024)

Cross Contamination with Other Products

Class IIILow

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

Abilify 30mg Tablets (Otsuka) – Product Contamination (2024)

Cross Contamination with Other Products

Class IIILow

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

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.

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

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

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

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

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