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. 2,763 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,763 in last 12 months

Showing 1668116700 of 30,153 recalls

Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Apollo Anesthesia Machine Recalled by Draeger Medical, Inc. Due to The...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2018· Helena Laboratories, Corp.

Recalled Item: Collagen Reagent Recalled by Helena Laboratories, Corp. Due to Through an...

The Issue: Through an investigation, it has been determined that vials of Collagen...

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

Class III — Low RiskOngoing
Medical DeviceMay 23, 2018· Helena Laboratories, Corp.

Recalled Item: Platelet Aggregation Kit Recalled by Helena Laboratories, Corp. Due to...

The Issue: Through an investigation, it has been determined that vials of Collagen...

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

Class III — Low RiskOngoing
Medical DeviceMay 23, 2018· Ortho Kinematics, Inc

Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...

The Issue: This email is to provide notification that, due to a software bug that has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2018· Steris Corporation

Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Recalled by Steris...

The Issue: The firm has become aware that the Reliance 1227 Cart and Utensil...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 45 mm Articulating Medium/Thick Reload with Tri-Staple Technology...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 45mm Gray Articulating Vascular Reload with Tri-Staple Technology...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· NewDeal SA

Recalled Item: TIBIAXYS Recalled by NewDeal SA Due to Use of the impacted product may cause...

The Issue: Use of the impacted product may cause a superficial infection requiring PO...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· NewDeal SA

Recalled Item: UNI-CP Recalled by NewDeal SA Due to Use of the impacted product may cause a...

The Issue: Use of the impacted product may cause a superficial infection requiring PO...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· NewDeal SA

Recalled Item: ADVANSYS MLP/DLP Recalled by NewDeal SA Due to Use of the impacted product...

The Issue: Use of the impacted product may cause a superficial infection requiring PO...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 45 mm Articulating Vascular/Medium Loading Unit with Tri-Staple...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 60 mm Articulating Medium/Thick Reload with Tri-StapleTechnology...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· NewDeal SA

Recalled Item: Large QWIX Recalled by NewDeal SA Due to Use of the impacted product may...

The Issue: Use of the impacted product may cause a superficial infection requiring PO...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 60 mm Articulating Vascular/Medium Loading Unit with Tri-Staple...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 60 mm Extra Thick Black Articulating Reload with Tri-Staple...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA 45 mm Extra Thick Black Articulating Reload with Tri-Staple...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2018· NewDeal SA

Recalled Item: ADVANSYS TTC Recalled by NewDeal SA Due to Use of the impacted product may...

The Issue: Use of the impacted product may cause a superficial infection requiring PO...

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

Class II — Potential Health HazardOngoing