Medical DeviceOct 3, 2018
Bausch + Lomb Stellaris Elite Vision Enhancement System, 23 ga recall — FDA Z-3270-2018
The back cap separates from the body of the vitrectomy cutter.
Class IIFDA: TerminatedBausch & Lomb Inc.
Latest records
Latest recalls — page 1353
The newest recall records with useful source details are listed here.
Medical DeviceOct 3, 2018
Philips Electronics Allura Xper F010/10 DRTable, System Code 722019 Vascular, cardiovascular recall — FDA Z-3235-2018
There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a…
Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceOct 3, 2018
Philips Electronics NTEGRIS Allura 9 0 FDXD, System Code 722498 Vascular, cardiovascular and recall — FDA Z-3220-2018
There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a…
Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceOct 3, 2018
Philips Electronics INTEGRIS Allura 15-12 (mono), System Code 722043 Vascular recall — FDA Z-3216-2018
There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a…
Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceOct 3, 2018
Biomet UK HipLOC Hip Fracture Fixation System- Hiploc System 130 Plate 38 mm Barrel 4 Hole recall — FDA Z-3261-2018
HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel
Class IIFDA: TerminatedBiomet UK Ltd.
Medical DeviceOct 3, 2018
Philips Electronics Allura Xper FD2O, System Code 722012 Vascular, cardiovascular and recall — FDA Z-3222-2018
There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a…
Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceOct 3, 2018
Bausch + Lomb Stellaris Elite Vision Enhancement System, 23 ga recall — FDA Z-3269-2018
The back cap separates from the body of the vitrectomy cutter.
Class IIFDA: TerminatedBausch & Lomb Inc.
Medical DeviceOct 3, 2018
Stryker GmbH Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #: HLRF recall — FDA Z-3240-2018
When creating a correction plan with the Correct Axial First button selected and the No. of corrections per day set to more than 1 (e.g., 2, 3, or 4), the Hexapod Software computes an…
Class IIFDA: TerminatedStryker GmbH
Medical DeviceOct 3, 2018
Philips Electronics INTEGRIS Allura 9 (biplane), System Code 722021 Vascular, cardiovascular recall — FDA Z-3214-2018
There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a…
Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceOct 3, 2018
Philips Electronics Allura Xper FD2O, System Code 722006 Vascular, cardiovascular and recall — FDA Z-3221-2018
There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a…
Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceOct 3, 2018
Philips Electronics AIIura Xper F010 DR Table, System Code 722022 Vascular, cardiovascular recall — FDA Z-3231-2018
There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a…
Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceOct 3, 2018
Philips Electronics INTEGRIS SUITE, System Code 722199 Vascular, cardiovascular and recall — FDA Z-3218-2018
There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a…
Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceOct 3, 2018
Bausch + Lomb Stellaris Elite Vision Enhancement System, 20 ga recall — FDA Z-3267-2018
The back cap separates from the body of the vitrectomy cutter.
Class IIFDA: TerminatedBausch & Lomb Inc.
Medical DeviceOct 3, 2018
Boston Scientific VALITUDE X4 CRT-P recall — FDA Z-3258-2018
Boston Scientific has identified a subset of active pacemaker and CRT-Ps systems with an elevated potential for early pacemaker replacement due to hydrogen-induced accelerated battery…
Class IIFDA: TerminatedBoston Scientific Corporation
Medical DeviceOct 3, 2018
GE Medical Systems Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the recall — FDA Z-3279-2018
GE Medical Systems has discovered a small area on the bore surface of the Discovery MR750w Nuclear Magnetic Resonance Imaging System, normally accessible to the patient, can get warm enough…
Class IIFDA: TerminatedGE Medical Systems, LLC
Medical DeviceOct 3, 2018
Biomet UK HipLOC Hip Fracture Fixation System-Hiploc System 140 Plate 38 mm Barrel 4 Hole recall — FDA Z-3264-2018
HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel
Class IIFDA: TerminatedBiomet UK Ltd.
Medical DeviceOct 3, 2018
Philips Electronics Poly C- DMCP-Visub(H3000), System Code 72238 Vascular, cardiovascular recall — FDA Z-3237-2018
There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a…
Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceOct 3, 2018
Philips Electronics Allura Xper FD1O C, System Code 722001 Vascular, cardiovascular and recall — FDA Z-3225-2018
There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a…
Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceOct 3, 2018
Philips Electronics INTEGRIS CV, System Code 722030 Vascular, cardiovascular and recall — FDA Z-3215-2018
There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a…
Class IIFDA: TerminatedPhilips Electronics North America Corporation
Medical DeviceOct 3, 2018
CooperSurgical Retractor System Elastic Stays recall — FDA Z-3278-2018
There is a possibility that the seal of the sterile pouch may be compromised, thereby increasing the risk of infection.
Class IIFDA: TerminatedCooperSurgical, Inc.
Medical DeviceOct 3, 2018
Biomet UK HipLOC Hip Fracture Fixation System-Hiploc System 135 Plate 38 mm Barrel 3 Hole recall — FDA Z-3262-2018
HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel
Class IIFDA: TerminatedBiomet UK Ltd.
Medical DeviceOct 3, 2018
Philips Electronics AIIuraXperFDlO/10, System Code 722011 Vascular, cardiovascular and recall — FDA Z-3230-2018
There is a potential for the Monitor Ceiling Suspension, which holds a large screen monitor, may detach from the actuator rotor shaft causing the monitor to fall from the ground. When a…
Class IIFDA: TerminatedPhilips Electronics North America Corporation
FoodOct 3, 2018
LOVE CORN USA Sea Salt , Net WT recall — FDA F-1987-2018
Love Corn Inc. is Initiating a voluntary recall for 1,404 cases of its 1.6 oz. Sea Salt Love Corn product, due to the presence of low levels of undeclared peanuts.
Class IIFDA: TerminatedLOVE CORN USA
FoodOct 3, 2018
Zakah Life Top Shelf White Maeng Da Premium Kratom, Zakah Life Dietary recall — FDA F-1984-2018
The firm distributes dietary supplements which contain Mitragyna speciosa (kratom) a dietary ingredient with inadequate information to provide reasonable assurance that such ingredient does…
Class IIFDA: TerminatedZakah Life LLC
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026243 records · 4 categoriesSeptember 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories