Medical DeviceJul 9, 2025
Philips XL14-3 Transducer recall — FDA Z-2068-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Monthly breakdown
2025 recalls by month
Select a month to review the recall records reported during that period.
December 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categoriesSeptember 2025285 records · 4 categoriesAugust 2025239 records · 4 categoriesJuly 2025370 records · 4 categoriesJune 2025342 records · 4 categoriesMay 2025258 records · 4 categoriesApril 2025302 records · 4 categoriesMarch 2025259 records · 4 categoriesFebruary 2025260 records · 4 categoriesJanuary 2025354 records · 4 categories
2025 recalls — page 79
Records are ordered by the best available source date.
Medical DeviceJul 9, 2025
Philips S8-3t Transducer recall — FDA Z-2061-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips X5-1 Transducer recall — FDA Z-2064-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips Respironics BiPAP V30 Auto Ventilator recall — FDA Z-2035-2025
This device does not indicate for use in patients with respiratory failure.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceJul 9, 2025
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 recall — FDA Z-2043-2025
Medline Industries, LP. is issuing a recall for specific Medline kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN which was identified that during insertion of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceJul 9, 2025
Valeda Light Delivery System Light Based Device for Dry Age Related Macular Degeneration recall — FDA Z-2046-2025
U.S. customers were shipped devices that were configured for the European Union and were unable to plug the device in the electrical outlet.
Class IIIFDA: OngoingLUMITHERA Inc.
Medical DeviceJul 9, 2025
Philips X7-2t Transducer recall — FDA Z-2066-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips 3D9-3v Transducer recall — FDA Z-2048-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips S7-2 Transducer recall — FDA Z-2059-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips S5-1 Transducer recall — FDA Z-2058-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Siemens Healthcare Diagnostics ADVIA 120/2120/2120i 3-in-1 TESTpoint Control (Norm Control) recall — FDA Z-2088-2025
Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceJul 9, 2025
VITROS XT 7600 Integrated System recall — FDA Z-2039-2025
a software anomaly allows test results to be reported using Micro Tip and Micro Slide diluent packs that the system treats as expired even when the Use Expired Reagents setting is not…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJul 9, 2025
Ortho-Clinical Diagnostics VITROS Chemistry Products OP Reagent Gen 15 recall — FDA Z-2073-2025
Lots from Generation (GEN) 15 of VITROS Chemistry Products OP Reagent may generate lower than expected quality control (QC) results. If the customer is unable to get passing quality control…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJul 9, 2025
Siemens Healthcare Diagnostics ADVIA 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control) recall — FDA Z-2089-2025
Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceJul 9, 2025
Philips V6-2 Transducer recall — FDA Z-2062-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips X8-2t Transducer recall — FDA Z-2067-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
HemoCue AB The HemoCue Glucose 201 Microcuvettes are designed for use with the HemoCue recall — FDA Z-2070-2025
Glucose microcuvettes experienced transit time outside of limits, so stability through the whole microcuvette lifetime can no longer be guaranteed. The affected products may not have been…
Class IIFDA: OngoingHemoCue AB
Medical DeviceJul 9, 2025
Philips X6-1 Transducer recall — FDA Z-2065-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips L12-3 Transducer recall — FDA Z-2054-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips C5-2 Transducer recall — FDA Z-2050-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips Respironics BiPAP A40 Ventilator recall — FDA Z-2037-2025
This device does not indicate for use in patients with respiratory failure.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceJul 9, 2025
Philips eL18-4 Transducer recall — FDA Z-2052-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
CORIN MEDICAL Apex Knee System. Model Numbers: KC-50090, KC-50097, KC-50110, KC-50117 recall — FDA Z-2069-2025
Investigation has identified that the age of the nylon packaging material has caused a loss of integrity of some pouches.
Class IIFDA: OngoingCORIN MEDICAL, LTD.
Medical DeviceJul 9, 2025
Maquet Critical Care AB Servo-u Ventilator System recall — FDA Z-2013-2025
Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active…
Class IFDA: OngoingMaquet Critical Care AB
About the 2025 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.