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Accriva Diagnostics, Inc.

Accriva Diagnostics, Inc. Recalls

All product recalls associated with Accriva Diagnostics, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

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 61–80 of 21319 recalls

Hemochron Activated Clotting Time Low-Range Test Cuvette,... (Accriva Diagnostics, Inc.) – foreign object (2025)

Test cuvettes, used with an assay for monitoring heparin anticoagulation, may have a foreign object that has sharp edges and could pose a risk of injury if not detected prior to handling.

Moderate

FDANov 5, 2025Nationwide• Accriva Diagnostics, Inc.

Oven Dried Fish (African Food on Wheels) – Botulinum Risk (2025)

Clostridium botulinum (uneviscerated fish)

Class IHigh

FDANov 5, 2025IN, NY• African Food on Wheels Inc.

Organic Moringa Leaf Powder (Africa Imports) – Salmonella Contamination (2025)

Salmonella

Product tested positive for Salmonella.

Class I

1 2 345 6...1066

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High

FDANov 4, 2025AZ, CA, IA +11 more• Africa Imports

Haagen-Dazs Mini Chocolate Ice Cream Bars (Dreyer's) – Undeclared Wheat (2025)

Undeclared Gluten

Undeclared wheat.

Class IIModerate

FDANov 3, 2025CA, KY, OH +1 more• Dreyer's Grand Ice Cream, Inc.

ViewPoint 6 (GE Healthcare) – incomplete patient history (2025)

GE HealthCare has become aware that the Patient History tab in ViewPoint 6 versions 6.15.3 and 6.15.4 ultrasound software may not include complete patient medical history information.

Moderate

FDANov 3, 2025Nationwide• GE Healthcare GmbH Oskar-Schlemmer-Str. 11 Munich Germany

IntelliVue Patient Monitor MX400 (Philips) – monitoring alarm issue (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue Patient Monitor MX600 (Philips) – Alarm Failure Risk (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

Stryker MV3 Bariatric Bed (Stryker) – Proximity Concern (2025)

Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together. These products have not been tested for compatibility and thus are not designed to be used together. The combination of both is not recommended by Stryker.

Moderate

FDAOct 31, 2025Nationwide• Stryker Medical Division of Stryker Corporation

IntelliVue MP80 (Philips) – monitoring alarm issue (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue Multi Measurement Server X2 (Philips) – monitoring alarm issue (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue Patient Monitor MX500 (Philips) – Alarm Failure Risk (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue Patient Monitor MX100 (Philips) – monitoring alarm issue (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue Patient Monitor MX800 (Philips) – Alarm Failure Risk (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue MP2 (Philips) – Alarm Failure Risk (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue MP5 (Philips) – Alarm Failure Risk (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue Patient Monitor MX700 (Philips) – Alarm Failure Risk (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue MP40 (Philips) – monitoring alarm issue (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

Micro Bird T-Series School Bus (Micro Bird) – Wheelchair Restraint Problem (2025)

Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2023-2026 G5 and 2025 T-Series school buses equipped with certain QRT-Deluxe and QRT-Max wheelchair restraints. The retractors may not lock, preventing the wheelchair from being properly secured.

High

NHTSAOct 31, 2025Nationwide• MICRO BIRD

IntelliVue MP70 (Philips) – Alarm Failure Risk (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc

IntelliVue MP30 (Philips) – monitoring alarm issue (2025)

Potential issue where the IntelliVue monitors did not alarm.

High

FDAOct 31, 2025Nationwide• Philips North America Llc