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FUJIFILM Healthcare Americas Corporation

FUJIFILM Healthcare Americas Corporation Recalls

All product recalls associated with FUJIFILM Healthcare Americas Corporation.

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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 2501–2520 of 10391 recalls

Surpria Software (FUJIFILM) – Scanning Error Risk (2022)

Error 00003050 or 00003052 may occur during scanning, the captured images will not be reconstructed and the Raw Data will not be displayed in the work list.result, may result in the need for additional scanning to capture the images properly for reconstruction, thereby exposing the patient to additional radiation

FDAJul 12, 2022Nationwide• FUJIFILM Healthcare Americas Corporation

SCENARIA View Software (FUJIFILM) – Scanning Error Risk (2022)

FDAJul 12, 2022Nationwide• FUJIFILM Healthcare Americas Corporation

SafeControl Handset (Wissner-Bosserhoff) – Reset Mode Concern (2022)

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When the handset is disconnected from the power mains, and mains operation is restored, the handset is reset to the preset Resident mode. In this mode, the backrest, legrest, and height adjustment can be moved.

FDAJul 11, 2022Nationwide• WISSNER-BOSSERHOFF GMBH Hauptstr. 4-6 Wickede (Ruhr) Germany

Lorazepam Injection 2mg (Hikma) – Compound Degradation (2022)

Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.

Class IIModerate

FDAJul 11, 2022Nationwide• Hikma Pharmaceuticals USA Inc.

Lorazepam Injection 4mg (Hikma) – Impurity Detection (2022)

Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.

Class IIModerate

FDAJul 11, 2022Nationwide• Hikma Pharmaceuticals USA Inc.

Lorazepam Injection 2mg (Hikma) – Impurity Concerns (2022)

Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.

Class IIModerate

FDAJul 11, 2022Nationwide• Hikma Pharmaceuticals USA Inc.

Ativan Injection (Hikma) – Compound Instability (2022)

Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.

Class IIModerate

FDAJul 11, 2022Nationwide• Hikma Pharmaceuticals USA Inc.

Pentacam HR (Oculus) – IOL Calculator Alignment Issue (2022)

Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs

FDAJul 8, 2022AL, AZ, AR +34 more• Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany

Pentacam AXL Wave (Oculus) – IOL Calculator Alignment Issue (2022)

Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs

FDAJul 8, 2022AL, AZ, AR +34 more• Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany

Pentacam AXL/HR (Oculus) – IOL Calculator Alignment Issue (2022)

Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs

FDAJul 8, 2022AL, AZ, AR +34 more• Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany

Cayden 9-Drawer Chests (Samson) – Tip-Over Entrapment Risk (2022)

This recall involves Samson International's Universal Broadmoore Cayden Gentleman's 9-drawer chests with model/item number M71C3180. The chests are brown and measure about 49 inches tall, 55 inches wide, and 18 inches deep. A label located on the back of each unit contains "Samson International," the model/item number, the month and year of manufacture, and the Costco customer item number 1335751. The chests are made of wood. The date codes are printed in MMDDYYYY (month/day/year) format and recalled units have manufacturing date codes between September 2019 and November 2019.

CPSCJul 7, 2022Nationwide• Lacquer Craft Mfg. Co., Ltd of China, a subsidiary of Samson Holding Ltd.

Fugleman UT10E and UT10X UTVs (Segway) – Fire Hazard (2022)

Fire/Burn Risk

This recall involves model year 2022 Fugleman UT10E and UT10X Utility Terrain Vehicles (UTVs). These vehicles were sold in various colors including white, black, gray and camo. "FUGLEMAN" decals are printed on the right and left rear side panels. The Segway logo is on the hood. The model number is located on the right and left rear side panels next to the Fugleman logo.

CPSCJul 7, 2022Nationwide• Segway Technology Co. Ltd., of China

Residential Gas-Fired Boilers (Laars) – carbon monoxide hazard (2022)

Fire/Burn Risk

This recall involves residential atmospheric gas-fired boilers manufactured from January 28, 2021 through January 12, 2022 and sold under the Laars Mini-Therm JX and Bradford White Brute Mini brand names. The following models and serial numbers are included and can be found on the boiler rating plate located on the on the right side of the boiler. Model Serial Number Range JX050 or BJX050 (Laars Mini-Therm JX) V21306297 through V22311517 JX075 or BJX075 (Bradford White Brute Mini) V21306262 through V21311453

CPSCJun 30, 2022Nationwide• Laars Heating Systems Company, of Rochester, New Hampshire

Lidocaine Cream (Mohnark) – child-resistant packaging (2022)

The recall involves Mohnark Pharmaceuticals Lidocaine 4% Topical Anesthetic Cream. The product was sold in a white tube with a flip-top closure. Mohnark Pharmaceuticals is printed under the blue and green logo on the right side of the product tube. The lot code is located at the bottom of the product tube. The affected lot codes are 01202201, 210201, 210301, 210503, 210505, 210601, 211002 and 210401. The UPC 860002324906 is located on bottom side panel of the packaging.

CPSCJun 30, 2022Nationwide• Mohnark Pharmaceuticals Inc., of Davie, Fla.

SX-One MicroKnife (SONEX HEALTH) – Dull Blade Potential (2022)

Potential of dull blade

FDAJun 29, 2022Nationwide• SONEX HEALTH LLC

Atellica CH Iron_2 (Siemens Healthcare) – Falsely Elevated Results (2022)

Falsely Elevated Atellica CH Microalbumin_2 (ALB_2) Results due to Reagent Carryover from the Iron_2 Assay. This defect occurs only when a microalbumin test is run immediately after an iron test.

FDAJun 28, 2022Nationwide• Siemens Healthcare Diagnostics, Inc.

HyVee Oven Baked Beans (Hy-Vee) – potassium sorbate excess (2022)

Baked bean product contains excessive amount of potassium sorbate

Class IIILow

FDAJun 28, 2022IL, IN, IA +6 more• Hy-Vee, Inc. dba Hy-Vee Fresh Commissary

Genesis II Non-Porous Tibial Baseplate (Smith & Nephew) – Mispackaged Product (2022)

The product was mispackaged (swapped). The devices within the inner tray matches the inner tray but does not match the outer box label and the chart sticks.

FDAJun 27, 2022Nationwide• Smith & Nephew, Inc.

HAMILTON-C6 Intensive Care Ventilator (Hamilton Medical) – Status Board Water Risk (2022)

Ventilator status indicator board can become loose, which could lead to water ingress (disinfectants) that may lead to technical fault alarms. Multiple technical faults in a short time may force ventilators into Safety Ventilation (blower runs constantly) or Ambient Sate (inspiratory channel/expiratory valves opened; patient breaths room air unassisted) with Panel connection lost message displayed

FDAJun 27, 2022Nationwide• Hamilton Medical AG Via Crusch 8 Bonaduz Switzerland

Nifedipine WSP Ointment 0.2% (Valor Compounding) – Potency Issue (2022)

Subpotent and Superpotent Drug

Class IHigh

FDAJun 27, 2022CA• Valor Compounding Pharmacy, Inc DBA Valor Compounding Pharmacy