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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 1661–1680 of 37661 recalls

SmartPath to dStream (Philips) – QBC seal failure (2025)

Laceration Risk

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.

High

FDAMar 24, 2025Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Peterbilt Model 220 (Peterbilt) – Propulsion System Issue (2025)

PACCAR Incorporated (PACCAR) is recalling certain 2022-2023 Peterbilt 220, 2024-2025 Peterbilt Model 220, and 2022-2025 Kenworth K270 and K370 Medium-Duty Battery Electric Vehicles. The cradle harness may have a loose electrical connection that can cause a loss of drive power.

High

NHTSAMar 24, 2025Nationwide• PETERBILT

ImmunoCard Crypto/Giardia Test (Medline) – Storage Temperature Concern (2025)

1...82 838485 86...1884

Page 84 of 1884Next

A single lot of the ImmunoCard STAT! Crypto/Giardia Test Kit was inadvertently stored in Medline warehouses at temperatures outside of the labeled storage requirements.

Low

FDAMar 24, 2025Nationwide• MEDLINE INDUSTRIES, LP Northfield

Voriconazole Tablets (Amerisource) – Supplier Notification (2025)

cGMP Deviations: Received notification from their supplier requesting they perform a recall due to the fact they repackaged the product.

Class IIModerate

FDAMar 24, 2025Nationwide• Amerisource Health Services LLC

Connex Accessory Power Management Stand (Baxter) – Battery Fire Risk (2025)

Fire/Burn Risk

There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter.

High

FDAMar 24, 2025Nationwide• Baxter Healthcare Corporation

Intera 1.5T R11 (Philips) – Coil Seal Adhesive Failure (2025)

Laceration Risk

High

FDAMar 24, 2025Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

DuraShock Aneroid Gauge (Baxter) – undeclared rubber band (2025)

Undeclared Allergen

Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

Low

FDAMar 21, 2025Nationwide• Baxter Healthcare Corporation

OEC 3D (GE Medical) – X-ray field distance issue (2025)

OEC Elite and OEC 3D Mobile C-Arms Exceeding 4% Source to Image Distance in X-ray Field.

Low

FDAMar 21, 2025Nationwide• GE Medical Systems, LLC

Connex Spot Monitor (Baxter) – undeclared rubber band (2025)

Undeclared Allergen

Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

Low

FDAMar 21, 2025Nationwide• Baxter Healthcare Corporation

Blood Pressure Cuff Kit (Baxter) – undeclared rubber band (2025)

Undeclared Allergen

Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

Low

FDAMar 21, 2025Nationwide• Baxter Healthcare Corporation

Connex Wall System (Baxter) – undeclared rubber band (2025)

Undeclared Allergen

Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

Low

FDAMar 21, 2025Nationwide• Baxter Healthcare Corporation

ABL90 Series (Radiometer) – analyzer freeze risk (2025)

ABL90 FLEX and ABL90 FLEX PLUS analyzers running with Radiometer Windows 10 versions RWIN10 1.0 and RWIN10 1.1 may unexpectedly freeze (the analyzer ceases to operate) during a sample measurement. The analyzer software includes a feature (watchdog) that detects a freeze and automatically restarts the software to continue operating the analyzer. However, even if a restart occurs, any sample being processed at that time will be lost, potential to lead to delay in test results.

Moderate

FDAMar 21, 2025AL, AZ, AR +46 more• Radiometer Medical ApS Akandevej 21 Bronshoj Denmark

Green Series 777 Wall System (Baxter) – undeclared rubber band (2025)

Undeclared Allergen

Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

Low

FDAMar 21, 2025Nationwide• Baxter Healthcare Corporation

CareStation 620 A1 (GE Healthcare) – ventilation ineffective (2025)

GE HealthCare has become aware that certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems will not provide effective ventilation in Volume Control Ventilation (VCV) mode. In these systems, effective ventilation can be achieved in Pressure Control Ventilation (PCV) or Pressure Control Ventilation Volume Guarantee (PCV-VG) modes or with Manual ventilation.

Moderate

FDAMar 21, 2025Nationwide• GE Medical Systems China Co., Ltd. Dev. Zone National Hi-Tech; No.

Spot Vital Signs 4400 (Baxter) – undeclared rubber band (2025)

Undeclared Allergen

Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

Low

FDAMar 21, 2025Nationwide• Baxter Healthcare Corporation

CareStation 750 A1 (GE Healthcare) – ventilation ineffective (2025)

Moderate

FDAMar 21, 2025Nationwide• GE Medical Systems China Co., Ltd. Dev. Zone National Hi-Tech; No.

International MV (International) – caliper suspension contact (2025)

International Motors, LLC (International) is recalling certain 2024 HV, 2020-2025 MV, and 2019 Workstar 7400 trucks. The caliper may contact a suspension spring or axle U-bolt and prevent the outer brake pad from functioning.

High

NHTSAMar 21, 2025Nationwide• INTERNATIONAL