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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands Recalls

All product recalls associated with PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 2101–2120 of 37661 recalls

Azurion 7 M12 (Philips) – Patient Fall Risk (2025)

Possibility of the patient falling from the table related to the mattress used on the patient table.

Moderate

FDAJan 13, 2025Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Duloxetine Capsules (Harvard Drug Group) – Nitrosamine Impurity (2025)

CGMP Deviations: presence of Nitrosamine Drug Substances Related Impurity (NDSRI), N-Nitroso-Duloxetine above the FDA recommended acceptable intake limit

Class IIModerate

FDAJan 13, 2025Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Shasta Oasis (Forest River) – Cooktop Safety (2025)

Fire/Burn Risk

Forest River, Inc. (Forest River) is recalling certain 2025 Shasta Oasis and Spirit travel trailers equipped with InVision Three Burner Cooktops. The aluminum burner tube may crack and cause a gas leak.

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High

NHTSAJan 13, 2025Nationwide• FOREST RIVER

Allura Xper FD20 (Philips) – Patient Fall Risk (2025)

Possibility of the patient falling from the table related to the mattress used on the patient table.

Moderate

FDAJan 13, 2025Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

AlluraXperFD20/15 (Philips) – Safety Issue (2025)

Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel

High

FDAJan 13, 2025Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Azurion 7 M12 (Philips) – Safety Issue (2025)

High

FDAJan 13, 2025Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

MediHoney Gel (Integra) – Seal Integrity (2025)

Potential that the induction seal is not completely sealed to the device tube packaging.

Moderate

FDAJan 10, 2025Nationwide• Integra LifeSciences Corp.

Nobel Biocare N1 TiUltra (Nobel) – Packaging Defect (2025)

Due to manufacturing issue (unintended by-product of the injection molding process) a sharp pin that may puncture the blister packaging and breaching the sterile barrier of the finished product.

High

FDAJan 10, 2025Nationwide• Nobel Biocare Vastra Hamngatan 1 Goteborg Sweden

Intact Vascular Tack System (Spectranetics) – Artery Treatment (2025)

Laceration Risk

Use of Tack Endovascular system, designed to treat acute dissections of inner wall or lining of an artery by tacking damaged tissue to inner luminal surface, could result in problems with deployment and stability of device in vessel after deployment, which may cause failure to resolve dissection, migration of implant, bailout stenting, reintervention, unintended removal of tack devices, and ischemia.

High

FDAJan 10, 2025Nationwide• Spectranetics Corporation

DxC 500 AU Analyzer (Beckman) – Stability Date Issue (2025)

Beckman Coulter has identified an issue which prevents the DxC 500 AU instrument from providing the correct onboard stability (Open Expiration) dates for assays that were loaded prior to a software upgrade (e.g. 1.3 to 1.4, 1.4 to 1.4.1, etc.). As a result, assays that have expired may still be used for sample processing, leading to inaccurate or erroneous patient test results. The issue only happens on assays loaded before instruments doing upgrades and does not impact new installation. It does not impact the assays loaded after upgrade.

High

FDAJan 10, 2025AL, CA, CO +16 more• BECKMAN COULTER LABORATORY SYSTEMS (SUZHOU) CO., LTD. No.

Granix Injection (Teva) – Failed Stability Test (2025)

Failed Stability Specifications - 12-month stability test result for one of the known peptides is below the specification limit

Class IIModerate

FDAJan 10, 2025Nationwide• Teva Pharmaceuticals USA, Inc

A820 myPTM Software (Medtronic) – App Interaction Delay (2025)

Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump.

Moderate

FDAJan 9, 2025Nationwide• Medtronic Neuromodulation

CircuitGuard Bacterial Filter (Kung Shin) – Airflow Blockage (2025)

The machine side connector of the filter HME may be occluded by plastic which prevents proper airflow. The issue may lead to ventilation bag malfunction in which the user is unable to inflate/deflate properly during manual ventilation. Potential risks to health include oxygen deprivation, leading to respiratory distress and medical complications.

Very High

FDAJan 9, 2025Nationwide• Kung Shin Plastics Co. Ltd. 65-2 Erh Chia Road Ying Kuo Town Taipei Hsien Taiwan

Medline Convenience Kits (Medline) – Skin Barrier Issue (2025)

Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.

Low

FDAJan 9, 2025CA, NY• MEDLINE INDUSTRIES, LP Northfield

CircuitGuard ThermoFlo (Kung Shin) – Airflow Blockage (2025)

Very High

FDAJan 9, 2025Nationwide• Kung Shin Plastics Co. Ltd. 65-2 Erh Chia Road Ying Kuo Town Taipei Hsien Taiwan

Soft Plum (AAHU BARAH) – Undeclared Sulfites (2025)

Undeclared Allergen

Product contains undeclared sulfites (4.66 mg/serving).

Class IIModerate

FDAJan 9, 2025CO, FL, GA +10 more• Global Commodities Inc

MSOT Acuity Echo (Ithera) – Safety Instruction (2025)

The MSOT Acuity Echo does not include an adequate instruction for safe operation of the device. The previous version of the user manuals contained a wrong value for the Nominal Ocular Hazard Distance (NOHD).

Moderate

FDAJan 8, 2025Nationwide• Ithera Medical Gmbh Zielstattstr. 13 Munich Germany

Stryker Precision Thin (Stryker) – Blade Measurement (2025)

Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.

Low

FDAJan 8, 2025Nationwide• Stryker Corporation

Clobazam Tablets (Amerisource) – Foreign Tablets (2025)

Presence of Foreign Tablets/Capsules

Class IIModerate

FDAJan 7, 2025Nationwide• Amerisource Health Services LLC

Guaifenesin Codeine Solution (PAI Holdings) – Superpotent Preservative (2025)

Superpotent; sodium benzoate preservative

Class IIILow

FDAJan 7, 2025OH• PAI Holdings, LLC. dba Pharmaceutical Associates Inc