Medical DeviceApr 24, 2024
Philips Ingenia Ambition S, Magnetic Resonance System recall — FDA Z-1568-2024
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 126
Records are ordered by the best available source date.
Medical DeviceApr 24, 2024
Philips Ingenia 3.0T, Magnetic Resonance System recall — FDA Z-1566-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Philips Intera 3.0T Quasar Dual, Magnetic Resonance System recall — FDA Z-1584-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Philips GYROSCAN T10-NT, Magnetic Resonance System recall — FDA Z-1560-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Ethicon STRATAFIX Spiral MONOCRYL Plus Bidirectional Knotless Tissue Control Device recall — FDA Z-1533-2024
Degraded and unusable upon removal from the foil pouch due to exposed environmental conditions during transit and storage, compromising sterility
Class IIFDA: OngoingEthicon, Inc.
Medical DeviceApr 24, 2024
Smiths Medical Model 3010 Syringe pumps: a recall — FDA Z-1542-2024
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 Ingenia 1.5T, Magnetic Resonance System recall — FDA Z-1563-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Philips SmartPath to dStream for XR and 3.0T, Magnetic Resonance System recall — FDA Z-1590-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Philips Respironics Trilogy Evo, all software versions except 1.05.06.00 recall — FDA Z-1504-2024
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 0.5T Standard, Magnetic Resonance System recall — FDA Z-1572-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Philips Respironics Garbin EVO, all software versions except 1.05.06.00 recall — FDA Z-1500-2024
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 1.5T Power/Pulsar, Magnetic Resonance System recall — FDA Z-1582-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Philips Respironics Trilogy EV300, all software versions except 1.05.06.00 recall — FDA Z-1502-2024
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 Ingenia Ambition X, Magnetic Resonance System recall — FDA Z-1569-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Philips MR 5300, Magnetic Resonance System recall — FDA Z-1587-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Elekta Disposable Biopsy Needle Kit for Leksell Stereotactic System, REF 911933, 2.1mm recall — FDA Z-1397-2024
Elekta has become aware that Disposable Biopsy Needles (911933) from one batch (837838839) can contain some microscopic debris on the inside of the biopsy needle. The material in the debris…
Class IFDA: OngoingElekta Instrument AB
Medical DeviceApr 24, 2024
Philips Achieva 3.0T for PET, Magnetic Resonance System recall — FDA Z-1554-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Philips SmartPath to dStream for 1.5T, Magnetic Resonance System recall — FDA Z-1589-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Smith & Nephew Medical RENASYS EDGE 300ML CANISTER WITH Solidifier- Indicated for patients recall — FDA Z-1596-2024
Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potentially causing damage to the pump
Class IIFDA: OngoingSmith & Nephew Medical, Ltd.
Medical DeviceApr 24, 2024
Philips Evolution Upgrade 3.0T, Magnetic Resonance System recall — FDA Z-1558-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Philips Intera 1.0T Power/Pulsar, Magnetic Resonance System recall — FDA Z-1574-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Cook Dilator - Coons Taper - Used for dilating puncture sites or catheter tracts for recall — FDA Z-1532-2024
Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility
Class IIFDA: OngoingCook Inc.
Medical DeviceApr 24, 2024
Philips Achieva 1.5T Initial, Magnetic Resonance System recall — FDA Z-1552-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceApr 24, 2024
Philips Intera 1.5T R11, Magnetic Resonance System recall — FDA Z-1583-2024
Patient support table floor plate may be incorrectly installed.
Class IIFDA: OngoingPhilips North America LLC
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.