Recalls affecting New York
Notices that name New York in their distribution area, plus every nationwide recall — nationwide recalls reach New York too.
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NHTSA safety recall · 7 months ago
Chrysler recall: A software error may cause the instrument panel display to fail
A software error may cause the instrument panel display to fail. As such, these vehicles fail to comply with the requirements of Federal Motor…
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Highest risk · 7 months ago
Vitaquest International Multiple Iron Supplement Bottles and Packets recall: Risk of Serious Injury or Death from Poisoning to Young Children
Risk of Serious Injury or Death from Poisoning to Young Children; Violates Mandatory Standard for Child-Resistant Packaging
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Highest risk · 7 months ago
Scubapro Monorail Weight Pockets for Buoyancy Compensator Devices recall: Risk of Serious Injury or Death from Drowning
Risk of Serious Injury or Death from Drowning
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Highest risk · 7 months ago
Prestige Import Group Supernova and Typhoon Lighters recall: Risk of Serious Injury or Death from Fire and Burn Hazards
Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Cigarette Lighters
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Highest risk · 7 months ago
Head USA Ski Boots recall: Risk of Serious Injury from Fall Hazard
Risk of Serious Injury from Fall Hazard
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Highest risk · 7 months ago
Bissell Over One Million Steam Shot OmniReach Steam Cleaners recall: Risk of Serious Burn Hazard from Attachments
Risk of Serious Burn Hazard from Attachments
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Class I · 7 months ago
Revitaderm, Tridergel Antiseptic wound care gel bottles and tubes recall: Products were found to contain Lysinibacillus fusiformis
Products were found to contain Lysinibacillus fusiformis, an environmental organism
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD10 recall: Philips has identified instances where X-ray imaging may not be initiated
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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Class II · 7 months ago
Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock recall: The outer packaging and blister pack labeling identify the product as 1mL
The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the…
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Class II · 7 months ago
Medtronic MiniMed, Inc. MiniMed 670G Insulin Pump recall: All Medtronic MiniMed infusion pumps (Paradigm series, 600 series
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and…
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Azurion 7 B12 recall: Philips has identified instances where X-ray imaging may not be initiated
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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Class II · 7 months ago
Synthes Products LLC 2.4 Volt TAP Cortex Screw TO 90MM recall: A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9
A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps…
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD10C recall: Philips has identified instances where X-ray imaging may not be initiated
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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Class II · 7 months ago
Medline Anterior HIP Pack Dynj64672B recall: Kits contain recalled Olympus biopsy valves. Olympus is investigating
Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the…
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Class II · 7 months ago
Medtronic MiniMed, Inc. MiniMed 700G Insulin Pump recall: All Medtronic MiniMed infusion pumps (Paradigm series, 600 series
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and…
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Class II · 7 months ago
ReCor Medical Inc. Brand Name: Paradise¿ Ultrasound Renal Denervation System Product recall: Due to firm distributing a nonconforming product that supposed to be scrapped
Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Vue Motion V12. Product Number: 1017979 recall: Potential that mis-ordered frames in Vue Motion during dynamic cine runs
Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Azurion 7 M20 recall: Philips has identified instances where X-ray imaging may not be initiated
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD20 recall: Philips has identified instances where X-ray imaging may not be initiated
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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Class II · 7 months ago
Burlington Medical, BAT Coverage recall: Potential for attenuation degradation over time, decreasing the lifespan
Potential for attenuation degradation over time, decreasing the lifespan.
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Class II · 7 months ago
Intuitive Surgical, Inc. Brand Name: da Vinci S, Si Tenaculum Forceps Instrument recall: Due to increased in complaints regarding frayed or broken pitch cables
Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
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Class II · 7 months ago
Burlington Medical, Kilt recall: Potential for attenuation degradation over time, decreasing the lifespan
Potential for attenuation degradation over time, decreasing the lifespan.
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD20/20 recall: Philips has identified instances where X-ray imaging may not be initiated
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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Class II · 7 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD20/15 recall: Philips has identified instances where X-ray imaging may not be initiated
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.