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. 2,715 recalls have been distributed to New York in the last 12 months.
Showing 17021–17040 of 55,896 recalls
Recalled Item: Synchron CX/DX/LX Beta-Hydroxybutyrate . in vitro diagnostic reagent....
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Beta-Hydroxybutyrate . in vitro diagnostic reagent. Recalled...
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beta-Hydroxybutyrate LiquiColor. in vitro diagnostic reagent. Recalled by...
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Beta-Hydroxybutyrate LiquiColor for Synchron CX/LX/DX. in...
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compounded Lyophilized Semorelin/Ipamorelin 3 mg For subcutaneous or...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Compounded Lyophilized AOD-9604 Recalled by Innoveix Pharmaceuticals Inc Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: COPAN FLOQSwabs Recalled by Copan Italia Due to A sterility assurance level...
The Issue: A sterility assurance level of 10-6 cannot be guaranteed due to intentional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUABEAM Handpiece Recalled by PROCEPT BIOROBOTICS CORPORATION Due to Scope...
The Issue: Scope tube tip may detach from the telescoping tube, which is attached to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIRCUL8 LUXE DVT PREVENTION DEVICE Recalled by Ortho8, Inc. Due to CIRCUL8...
The Issue: CIRCUL8 LUXE DVT PREVENTION DEVICE is marketed without FDA clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVEXIA LUXE DVT PREVENTION DEVICE Recalled by Ortho8, Inc. Due to EVEXIA...
The Issue: EVEXIA LUXE DVT PREVENTION DEVICE is marketed without FDA clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards PediaSat Oximetry Catheter Set Recalled by Edwards Lifesciences, LLC...
The Issue: There is a potential for internal leaks within catheters.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards PediaSat Oximetry Catheter Set Recalled by Edwards Lifesciences, LLC...
The Issue: There is a potential for internal leaks within catheters.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards PediaSat Oximetry Catheter Kit Recalled by Edwards Lifesciences, LLC...
The Issue: There is a potential for internal leaks within catheters.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards PediaSat Oximetry Catheter Kit Recalled by Edwards Lifesciences, LLC...
The Issue: There is a potential for internal leaks within catheters.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards PediaSat Oximetry Catheter Set Recalled by Edwards Lifesciences, LLC...
The Issue: There is a potential for internal leaks within catheters.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards PediaSat Oximetry Catheter Kit Recalled by Edwards Lifesciences, LLC...
The Issue: There is a potential for internal leaks within catheters.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scorpion Portal Vein Access Set - Product Usage: used to Recalled by Argon...
The Issue: As a result of design changes, sheaths have exhibited cracking/breaking at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX Recalled...
The Issue: Due to failure to acquire pre-market clearance for its high resolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zippie Voyage Recalled by Sunrise Medical (US) LLC Due to The seating system...
The Issue: The seating system unexpectedly detached, which resulted in the seating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zippie Voyage Recalled by Sunrise Medical (US) LLC Due to The seating system...
The Issue: The seating system unexpectedly detached, which resulted in the seating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.