Medical DeviceApr 24, 2024
Philips Achieva 1.5T Conversion, Magnetic Resonance System recall — FDA Z-1551-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Monthly breakdown
2024 recalls by month
Select a month to review the recall records reported during that period.
December 2024325 records · 4 categoriesNovember 2024355 records · 4 categoriesOctober 2024409 records · 4 categoriesSeptember 2024547 records · 4 categoriesAugust 2024327 records · 4 categoriesJuly 2024318 records · 4 categoriesJune 2024286 records · 4 categoriesMay 2024422 records · 4 categoriesApril 2024323 records · 4 categoriesMarch 2024332 records · 4 categoriesFebruary 2024425 records · 4 categoriesJanuary 2024298 records · 4 categories
2024 recalls — page 127
Records are ordered by the best available source date.
Medical DeviceApr 24, 2024
Siemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models: Artis zee floor recall — FDA Z-1598-2024
Coolant level in the cooling circuit drops below a certain level, this may result in a situation in which the X-ray tube is no longer sufficiently cooled and the system will display the…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Medical DeviceApr 24, 2024
Masimo Rad-G, Pulse Oximeter (W/Patient Cable), REF:9849, Rx Only recall — FDA Z-1538-2024
Their is a potential that Oximeter may automatically power off and on resulting in loss of monitoring.
Class IIFDA: OngoingMasimo Corporation
Medical DeviceApr 24, 2024
Philips Respironics Trilogy Evo O2, all software versions except 1.05.06.00 recall — FDA Z-1503-2024
Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceApr 24, 2024
Philips Intera CV, Magnetic Resonance System recall — FDA Z-1586-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Smiths Medical Medfusion Model 3500 Syringe pumps, Item Numbers: a) 3500 b) 3500-0600-00 c) recall — FDA Z-1540-2024
Medfusion Model 4000, 3500, and 3010 pumps manufactured or serviced with Barrel Clamp Guide (Part Number G6000716), Lot Numbers P0407365, P0486670, and P0561740 may contain a molding defect…
Class IIFDA: OngoingSmiths Medical ASD Inc.
Medical DeviceApr 24, 2024
Philips Achieva 3.0TX for PET, Magnetic Resonance System recall — FDA Z-1555-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Philips Intera Achieva 1.5T Pulsar, Magnetic Resonance System recall — FDA Z-1585-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Philips GYROSCAN T5, Magnetic Resonance System recall — FDA Z-1561-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Philips MR 7700, Magnetic Resonance System recall — FDA Z-1588-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Cook Trocar Needle - Used for dilating puncture sites or catheter tracts for percutaneous recall — FDA Z-1526-2024
Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility
Class IIFDA: OngoingCook Inc.
Medical DeviceApr 24, 2024
Cook Yueh Centesis Disposable Catheter Needle - Intended for use in percutaneous fluid recall — FDA Z-1527-2024
Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility
Class IIFDA: OngoingCook Inc.
Medical DeviceApr 24, 2024
Philips Enterprise 1.5T, Magnetic Resonance System recall — FDA Z-1557-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Philips Ingenia Elition X, Magnetic Resonance System recall — FDA Z-1571-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Masimo Rad-G, Pulse Oximeter with temperature (W/Sensor), REF:9210, Rx Only recall — FDA Z-1536-2024
Their is a potential that Oximeter may automatically power off and on resulting in loss of monitoring.
Class IIFDA: OngoingMasimo Corporation
Medical DeviceApr 24, 2024
Cook Entuit Secure Adjustable Gastrointestinal Suture Anchor Set - Intended for anchoring recall — FDA Z-1529-2024
Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility
Class IIFDA: OngoingCook Inc.
Medical DeviceApr 24, 2024
Conformis Identity Imprint PS Tibial Tray Size 4: Lot 540287 recall — FDA Z-1591-2024
Size 5 Tibial Tray from Lot 508287 was packaged in a Size 4 box from Lot 540287. It was confirmed that Lot 540287 and Lot 508287 were swapped between the pouching and final pack.
Class IIFDA: OngoingConformis, Inc.
Medical DeviceApr 24, 2024
Philips Respironics Aeris EVO, all software versions except 1.05.06.00 recall — FDA Z-1499-2024
Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceApr 24, 2024
Philips Respironics LifeVentEVO2, all software versions except 1.05.06.00 recall — FDA Z-1501-2024
Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceApr 24, 2024
Cook Dilator - Intended to be used for dilating puncture sites or catheter tracts for recall — FDA Z-1530-2024
Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility
Class IIFDA: OngoingCook Inc.
Medical DeviceApr 24, 2024
Baxter Healthcare Surgical Tools and Cardiovascular Specialty marketing brochures, Reference recall — FDA Z-1524-2024
The Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceApr 24, 2024
SonarMed AW-S030 NEO SONARMED SENSOR 3.0MM recall — FDA Z-1520-2024
The failure to detect the partial obstruction in a 2.5mm sensor.
Class IFDA: OngoingSonarMed Inc.
Medical DeviceApr 24, 2024
Philips Intera 1.5T Explorer/Nova Dual, Magnetic Resonance System recall — FDA Z-1579-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Cook Peel-Away Introducer - Intended for the percutaneous introduction of balloon, electrode recall — FDA Z-1528-2024
Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility
Class IIFDA: OngoingCook Inc.
About the 2024 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.