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. 2,704 recalls have been distributed to New York in the last 12 months.
Showing 19361–19380 of 30,153 recalls
Recalled Item: INTENSIA Models: VR 124 Recalled by Sorin Group Italia SRL - CRF Due to...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OVATIO Models: VR 6250 Recalled by Sorin Group Italia SRL - CRF Due to Sorin...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PARADYM Models: VR 8250 Recalled by Sorin Group Italia SRL - CRF Due to...
The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit...
The Issue: The current secondary packaging, a box, incorrectly states that the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys PreciControl Varia 3 Recalled by Roche Diagnostics Corporation Due...
The Issue: e-barcode and value sheet for PreciControl Varia contains a typographical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eMAG System Recalled by bioMerieux, Inc. Due to Some anomalies have been...
The Issue: Some anomalies have been identified during manufacturing controls.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CytoGuard Closed Luer Connector Recalled by B Braun Medical Inc Due to B....
The Issue: B. Braun is voluntarily recalling 13 lots of CytoGuard Closed Luer Connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPoint¿ 500 Blood Gas Analyzer with v2.4 software for professional...
The Issue: Potential Patient Demographic Error with Blank Patient ID Field
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Optetrak Logic CC 15mm Tibial Augment Screws Recalled by Exactech,...
The Issue: Missing Screw in carton. Nine (9) serial numbers were identified as being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fellows "Mighty 8" Power strip (Part Number 04175-0008) and TrippLite...
The Issue: Merge is conducting a hardware recall (replacement) of Fellows "Mighty 8"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The JETSTREAM is a rotational atherectomy catheter system designed for...
The Issue: Boston Scientific is initiating a voluntary removal of two lots of JETSTREAM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for Recalled...
The Issue: Complaints concerning kinked haptics that were occurring during lens delivery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroVue CIC-C1q EIA Recalled by Diagnostic Hybrids, Inc. Due to There is a...
The Issue: There is a potential for the slope of the standard curve to fail to meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mederi Stretta Catheter and Accessory Kit Recalled by Mederi Therapeutics,...
The Issue: Product sterility compromised due to breach in sterile barrier package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between...
The Issue: The second generation neoBLUE 2 lights with a black band, sold from 2003 to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solus Flexible wire-reinforced laryngeal mask airways under the following...
The Issue: A defect in the wire-reinforced tubing may result in a partial of total...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter has confirmed that the Export feature located in the Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATAR Disposable Extension Cable Recalled by Oscor, Inc. Due to The Reusable...
The Issue: The Reusable Oscor ATAR extension cables could separate from the connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi EndoWrist Suction Irrigator Recalled by Intuitive Surgical, Inc....
The Issue: Intuitive Surgical has become aware that in specific scenarios with system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATAR Reusable Extension Cable Recalled by Oscor, Inc. Due to The Reusable...
The Issue: The Reusable Oscor ATAR extension cables could separate from the connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.