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. 2,771 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,771 in last 12 months

Showing 1640116420 of 30,153 recalls

Medical DeviceJuly 13, 2018· Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical

Recalled Item: Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution...

The Issue: Immersion time stated on the bottle is 45 minutes while the product...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Tosoh Bioscience Inc

Recalled Item: G8 Automated HPLC Analyzer - 723G8 Product Usage - In Recalled by Tosoh...

The Issue: Analyzers were distributed with software which lacks a 510K

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 2008T HEMODIALYSIS SYSTEM W/BIBAG Recalled by Fresenius Medical Care Renal...

The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 2008T HEMODIALYSIS SYS Recalled by Fresenius Medical Care Renal Therapies...

The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Smiths Medical ASD Inc.

Recalled Item: Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin...

The Issue: The product was mislabeled with the incorrect label.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJuly 13, 2018· Exactech, Inc.

Recalled Item: Tibial Alignment Guide Recalled by Exactech, Inc. Due to Exactech is...

The Issue: Exactech is recalling the Tibial Alignment Guide because the Global Trade...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Haemonetics Corporation

Recalled Item: Haemonetics OrthoPAT System-Integrated Set. Product Code: 1150H-00 OrthoPAT...

The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Haemonetics Corporation

Recalled Item: Haemonetics¿ OrthoPAT¿ System-OPAT QuickConnect Reservoirs. Product Code:...

The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VM 3/4/6/8 Patient Monitors Recalled by Philips...

The Issue: Philips has received several reports in which monitors with lithium ion...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VSV (Vital Signs Viewer) Recalled by Philips Electronics...

The Issue: Philips has received several reports in which monitors with lithium ion...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VS4 Vital Signs Monitor Recalled by Philips Electronics...

The Issue: Philips has received several reports in which monitors with lithium ion...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VS2 monitor Recalled by Philips Electronics North America...

The Issue: Philips has received several reports in which monitors with lithium ion...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VS3 Vital Signs Monitor Recalled by Philips Electronics...

The Issue: Philips has received several reports in which monitors with lithium ion...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· GE Healthcare, LLC

Recalled Item: Revolution CT systems with the SmartStep Option The system is Recalled by GE...

The Issue: On the Revolution CT systems equipped with the SmartStep Option, the Z...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Ultradent Products, Inc.

Recalled Item: Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Recalled by...

The Issue: Dental varnish has the possibility of having an unpleasant and off flavor.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right Recalled...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left Recalled by...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Right Recalled...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right Recalled by...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Left Recalled by...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing