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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

620

Class I (Serious)

Most Recent

Dec 2025

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 901–920 of 10937 recalls

Philips Azurion Interventional Fluoroscopic X-ray System ... (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands) – potential loss of imaging (x-ray) fun... (2024)

Potential Loss of Imaging (X-ray) Functionality and/or Longer Time to Perform Cold Restart

FDAJul 15, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Proteus XR/a X-Ray System (GE Healthcare) – Missing Manual (2024)

The XR system, Proteus XR/a, does not have a de-installation manual describing process steps for de-installing the devices. De-installation instruction process steps must be followed when de-installing these devices to avoid personnel injury during de-install.

FDAJul 12, 2024Nationwide• GE Healthcare (China) Co., Ltd. 1F-5F BLD 1, No.1 Tongji South Road, Beijing Economic-Technological Development Area Beijing China

Proton Therapy System (IBA) – Positioning System Issue (2024)

Temporary deactivation of collision detection for Forte Robotic Patient Positioning System occasionally experiences issues

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FDAJul 10, 2024IL, LA, MI +6 more• Ion Beam Applications S.A. Chemin Du Cyclotron 3 Ottignies-Louvain-La-Neuve Belgium

Guidewire (Bard Peripheral Vascular) – Misassembly Risk (2024)

Due to guidewires being manufactured incorrectly with the guidewires being mis-assembled within the hoop such that the proximal (stiff) end of the guidewire is located at the distal end of the hoop. Injury could occur if the user attempts to insert the proximal end into the patient.

FDAJul 10, 2024Nationwide• Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438

Aurora 7 Lighthead (DKK Dai-Ichi) – Weld Frame Crack (2024)

The weld on the light head frame can crack which could lead to problems such as the light head frame sagging, the plastic front face housing cracking, or the light head detaching.

FDAJul 9, 2024Nationwide• DKK Dai-Ichi Shomei Co., Ltd. 1 Chome 32-26 Sakashita Itabashi Japan

DLP Venous Cannulae (Medtronic) – Incorrect Product Placement (2024)

During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312).

FDAJul 9, 2024Nationwide• Medtronic Perfusion Systems

Aurora 4 Lighthead (DKK Dai-Ichi) – Weld Frame Crack (2024)

The weld on the light head frame can crack which could lead to problems such as the light head frame sagging, the plastic front face housing cracking, or the light head detaching.

FDAJul 9, 2024Nationwide• DKK Dai-Ichi Shomei Co., Ltd. 1 Chome 32-26 Sakashita Itabashi Japan

Aurora 2 Lighthead (DKK Dai-Ichi) – Weld Frame Crack (2024)

The weld on the light head frame can crack which could lead to problems such as the light head frame sagging, the plastic front face housing cracking, or the light head detaching.

FDAJul 9, 2024Nationwide• DKK Dai-Ichi Shomei Co., Ltd. 1 Chome 32-26 Sakashita Itabashi Japan

Aurora 3 Lighthead (DKK Dai-Ichi) – Weld Frame Crack (2024)

The weld on the light head frame can crack which could lead to problems such as the light head frame sagging, the plastic front face housing cracking, or the light head detaching.

FDAJul 9, 2024Nationwide• DKK Dai-Ichi Shomei Co., Ltd. 1 Chome 32-26 Sakashita Itabashi Japan

Shelled Walnuts (Stutz) – Listeria Detected (2024)

Listeria

Shelled walnuts tested positive for Listeria

Class IHigh

FDAJul 8, 2024AZ, TX• Stutz Packing Company

ENT Cutting Bur (Medtronic Xomed) – Expired Distribution (2024)

Product was distributed past expiration date.

FDAJul 5, 2024Nationwide• Medtronic Xomed, Inc.

FRT250 Cartridge (Pega Medical) – Incorrect Component (2024)

During the assembly of the FRT250 cartridge assembly, an incorrect component was used. Specifically, the FRT240-HEX (2) was used instead of the FRT250-HEX.

FDAJul 4, 2024Nationwide• ORTHOPEDIATRICS CANADA ULC Dba PEGA MEDICAL 1111 Chomedey (A-13) E Laval Canada

PEG-3350 Solution (Lupin) – Defective Container (2024)

Defective container: potential for non-sealed pouches which can lead to product leakage.

Class IIILow

FDAJul 2, 2024Nationwide• Novel Laboratories, Inc. d.b.a Lupin Somerset

Daikin FIT Heat Pumps (Daikin) – potential equipment failure (2024)

This recall involves Daikin FIT, Amana Brand S-series, and Goodman SD heat pumps that provide heating and cooling. The recalled units are beige and the model name is printed on the outside of the unit. The model number is located on the serial plate on the side of the unit. The following model numbers are included in this recall: Recalled Daikin FIT Recalled Amana S-Series Recalled Goodman SD DZ6VSA1810-AA ASZS601810-AA GSZS601810-AB DZ6VSA1810-AB ASZS601810-AB GSZS602410-AB DZ6VSA2410-AA ASZS602410-AA GSZS603010-AB DZ6VSA2410-AB ASZS602410-AB GSZS603610-AB DZ6VSA241E-AB ASZS60241E-AB DZ6VSA3010-AA ASZS603010-AA DZ6VSA3010-AB ASZS603010-AB DZ6VSA3610-AA ASZS603610-AA DZ6VSA3610-AB ASZS603610-AB

CPSCJun 27, 2024Nationwide• Daikin Comfort Technologies Manufacturing L.P., of Houston, Texas

Co-op Cycles REV Bicycles (REI) – fall injury hazard (2024)

This recall involves REI Co-op Cycles REV 12-, 16-, or 20-inch kid's bicycles (all model years 2022-2024). Serial numbers included in the recall begin with "ET22," "ET23," "01VX" or "07VX." The serial number is printed underneath the bike frame on the bottom bracket or down tube. Brand Model SKU/Article # Color Co-op Cycles REV 12 Kids Bike 190741 BONDI (green) Co-op Cycles REV 12 Kids Bike 190741 PENCIL (yellow) Co-op Cycles REV 16 Kids Bike 190742 SURFS UP (blue) Co-op Cycles REV 16 Kids Bike 190742 CATCH UP (red) Co-op Cycles REV 16 Kids Bike 190743 FOUR LEAF (green) Co-op Cycles REV 20 Kids Bike 190743 PLUM BURST (purple)

CPSCJun 27, 2024Nationwide• RECREATIONAL EQUIPMENT INC. (REI), of Sumner, Washington

Premo Turkey & Swiss (Lipari Foods) – Salmonella Contamination (2024)

Salmonella

Potential contamination with Salmonella

Class IIModerate

FDAJun 27, 2024AL, AR, FL +13 more• Lipari Foods Operating Company, LLC.

Premo King Club Footlong (Lipari Foods) – Salmonella Contamination (2024)

Salmonella

Potential contamination with Salmonella

Class IIModerate

FDAJun 27, 2024AL, AR, FL +13 more• Lipari Foods Operating Company, LLC.

Premo Meat Lovers (Lipari Foods) – Salmonella Contamination (2024)

Salmonella

Potential contamination with Salmonella

Class IIModerate

FDAJun 27, 2024AL, AR, FL +13 more• Lipari Foods Operating Company, LLC.

Ventana Anti-CD10 Antibody (Ventana) – Staining Inaccuracy (2024)

Their is a potential for high background and off-target staining when using the monoclonal primary antibody which can result in false positive results.

FDAJun 27, 2024Nationwide• Ventana Medical Systems, Inc.

DVOT Multi-Pathogen Antigen Test (Feng Chun Yuan) – Unauthorized Sales (2024)

The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.

FDAJun 26, 2024Nationwide• FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN) CO., LTD No. 1304 Science And Technology Innovation Park, Shajing Dahong Shenzhen China