Product Recalls in New York
Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,659 recalls have been distributed to New York in the last 12 months.
Showing 25381–25400 of 30,153 recalls
Recalled Item: Coat-A-Count Direct Androstenedione Recalled by Siemens Healthcare...
The Issue: The assay is demonstrating a higher frequency of results greater than 10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MC-500 Multicolor Laser Photocoagulator Recalled by Nidek Inc Due to Laser...
The Issue: Laser aperture label was not affixed to device prior to shipment in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDC Anaerobe 5% Sheep Blood Agar CDC Anaerobe 5% Sheep Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Medical System Allura Xper X-Ray Angiographic Recalled by Philips...
The Issue: In certain circumstances, a software error can lead to a situation where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM) // Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Qube Compact Monitor Recalled by Spacelabs Healthcare...
The Issue: Spacelabs Healthcare is recalling Qube Compact Monitor, Model 91390, due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Hospira MedNet Medication Management Suite (MMS). Product Usage: The...
The Issue: Hospira MedNet 5.5, 5.8.1, and 5.8.2 contains software defect where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA Digital Radiography X-Ray system DX-D 100 Agfa's DX-D 100 Recalled by...
The Issue: When liquid comes in contact with the DX-D 100 touch screen, the device may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Columbia Agar with 5% Sheep Blood Columbia Agar with 5% Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Canto and associated Fluidics Cart Product Usage: Flow Recalled by...
The Issue: Laser cooling fans and internal fan of the associated fluidics cart are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the...
The Issue: The seals of the respiratory gas humidifier adaptor packaging may be creased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DMI Duro-Med Industries Rollator Transport Chair Recalled by Briggs Medical...
The Issue: There have been 5 customer reports of a 501-1018 series DMI Rollator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aqua 540 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humidifier Adaptor 040 Recalled by Teleflex Medical Due to The seals of the...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adaptor Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraStream Chronic Hemodialysis Catheter Standard Kit Recalled by Argon...
The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraStream Peel Away Kit Recalled by Argon Medical Devices, Inc Due to...
The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraStream Exchange Kit Model Numbers 32001524 (24 cm) Recalled by Argon...
The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.