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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)

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 4801–4820 of 25000 recalls

2D Perfusion (Philips) - Signal Processing (2023)

There are technical issues related to signal generation and processing, which can lead to inaccurate presentations.

Moderate

FDAFeb 20, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

SmartPerfusion (Philips) - Signal Processing (2023)

There are technical issues related to signal generation and processing, which can lead to inaccurate presentations.

Moderate

FDAFeb 20, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Enfamil ProSobee Powder (Mead Johnson) – Voluntary batch removal (2023)

Reckitt, a producer of nutrition products, announced today that out of an abundance of caution, it has chosen to voluntarily recall two (2) select batches of ProSobee 12.9 oz. Simply Plant-Based Infant Formula due to a remote possibility of cross-contamination with Cronobacter sakazakii.

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Class IHigh

FDAFeb 19, 2023AL, AK, AZ +36 more• Mead Johnson & Company

Raystation Treatment Planning (RaySearch) - Collimator Angle (2023)

It is possible to set a non-zero collimator angle in the Virtual Simulation module. The angle will be correct in the user interface but if the plan is DICOM exported by using the VSIM Export button, the angle will not be correct in the exported RT plan. In the exported RT plan, the DICOM attribute Beam Limiting Device Angle (300A,0120) is set to zero, regardless of the selected collimator angle.

Moderate

FDAFeb 17, 2023Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

Arjo Portable Scale Adaptor (Arjohuntleigh) - Strap Detachment (2023)

Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach.

Moderate

FDAFeb 17, 2023NY, OH• Arjohuntleigh Magog, Inc.

Gabapentin Tablets (Sciegen) – tablet mix-up (2023)

Presence of Foreign Tablets/Capsules: Pharmacist reported presence of some Gabapentin tablets 800 mg comingled in Gabapentin 600 mg 500 count bottles.

Class IIILow

FDAFeb 17, 2023Nationwide• Sciegen Pharmaceuticals Inc

Dibucaine Hemorrhoidal Ointment (Akron Pharma) – labeling error (2023)

Labeling: Incorrect or Missing Lot and/or Exp Date

Class IIILow

FDAFeb 17, 2023Nationwide• Akron Pharma, Inc.

Thermage CPT System (Solta Medical) - Calibration Problem (2023)

A service unit was potentially improperly tested and calibrated during manufacturing on a failed test station.

Moderate

FDAFeb 16, 2023MD• Solta Medical Inc

ElectraMeccanica Solo G3 (ElectraMeccanica) - Inverter Defect (2023)

Electra Meccanica Vehicles Corp (Electra) is recalling certain 2019 Solo G2 and 2021-2023 Solo G3 vehicles. A defect in the motor controller and inverter or the battery controller may cause the electric motor to shut down and cause a sudden loss of drive power.

Moderate

NHTSAFeb 16, 2023Nationwide• ELECTRAMECCANICA

Paradise Grills Outdoor Kitchens – Fire hazard (2023)

Fire/Burn Risk

This recall involves First Generation Paradise Grills Outdoor Kitchens. They can have cabinets, sinks, refrigerators, and other features such as LED lighting, Tiki Huts, commercial grills, granite and other additional options. The recalled models are the GX-3, GX-4, GX-5, GX-6, GX-7, GX-8, GX-9, GX-10, GX-11 GX12 and GX14, Tahiti, Fiji, Tropicana, Aruba 6 and Aruba 8. The model name is listed on the sales agreement.

High

CPSCFeb 16, 2023Nationwide• Paradise Grilling Systems Inc., of Ocoee, Florida

Infinity Occipitocervical Screw (Medtronic) - Material Strength (2023)

Incorrect type of titanium was used which reduces the gripping strength of the screw head of 5 batches of Infinity Multi-Axial Screws

Moderate

FDAFeb 16, 2023Nationwide• Medtronic Sofamor Danek USA Inc

Flex-Neck Catheter Kit (Merit) - Unintended Distribution (2023)

Product that was built for design verification testing was inadvertently distributed to customers.

Moderate

FDAFeb 15, 2023Nationwide• Merit Medical Systems, Inc.

FoundationOne CDx (Foundation Medicine) - Claim Error (2023)

An incorrect negative claim was identified on the claims page; the device variant information was displayed correctly in the tumor profiling section of the FDA-approved test report.

Moderate

FDAFeb 15, 2023Nationwide• Foundation Medicine, Inc.

Testosterone Cypionate Injection (Azurity) – Crystal Redissolution Issue (2023)

cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.

Class IIModerate

FDAFeb 15, 2023Nationwide• Azurity Pharmaceuticals, Inc.

Warfarin Sodium Tablets (Rising Pharmaceuticals) – Impurities Spec Failure (2023)

Failed Impurities/Degradation Specifications

Class IIModerate

FDAFeb 15, 2023Nationwide• RISING PHARMACEUTICALS

Buprenorphine Patch (AVEVA) – impurity specification failure (2023)

Failed Impurities/Degradation Specifications: Out of specification for related substance 10-hydroxy buprenorphine N-Oxide results generated at the 18-month stability timepoint.

Class IIILow

FDAFeb 15, 2023Nationwide• AVEVA Drug Delivery Systems, Inc.

Buprenorphine Transdermal System (AVEVA) – Substance Impurity Concerns (2023)

Failed Impurities/Degradation Specifications: Out of specification for related substance 10-hydroxy buprenorphine N-Oxide results generated at the 18-month stability timepoint.

Class IIILow

FDAFeb 15, 2023Nationwide• AVEVA Drug Delivery Systems, Inc.