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 25601–25620 of 55,896 recalls
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...
The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Recalled...
The Issue: There is a potential of fracture, bending or shearing of the driver.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...
The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T7 Driver Solid AO (Part Number 110018541) Product Usage: The Recalled by...
The Issue: There is a potential of fracture, bending or shearing of the driver.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edamame Salad sold under the following labels: BOSTON SALADS Prepared...
The Issue: Possible metal fragment contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lee's Tea brand of Pink Chai - Organic Spiced Tulsi Recalled by LEE'S...
The Issue: Product may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sea Salt 70% Dark Chocolate 3 oz. bars Recalled by Theo Chocolate Inc Due to...
The Issue: Theo Chocolate Sea Salt 70% Dark Chocolate Bar is recalled due to undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EZ Derm Porcine Xenograft Recalled by Molnlycke Health Care, Inc Due to...
The Issue: Intermittent heat seal failures on the outer pouch of some EZ Derm products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thallous Chloride TI 201 Injection Recalled by Medi-Physics Inc. dba GE...
The Issue: Chemical Contamination: Trace amounts of an impurity was detected in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenobarbital Oral Solution Recalled by Lohxa LLC Due to Labeling: Incorrect...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - the label contains an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pravastatin Sodium Tablets USP Recalled by Glenmark Pharmaceuticals Inc.,...
The Issue: Presence Of Foreign Tablet: in a bottle of Pravastatin Sodium Tablets 20 mg.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bismuth Subsalicylate Oral Suspension 262mg/15mL Recalled by Lohxa LLC Due...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - the label contains an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Canon Aquilion Precision Recalled by Canon Medical System, USA, INC. Due to...
The Issue: Scanning may be interrupted due to an error during execution of the eXam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Aquilion One Vision Recalled by Canon Medical System, USA, INC. Due to...
The Issue: Scanning may be interrupted due to an error during execution of the eXam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Aquilion Premium Recalled by Canon Medical System, USA, INC. Due to...
The Issue: Scanning may be interrupted due to an error during execution of the eXam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Aquilion One Recalled by Canon Medical System, USA, INC. Due to...
The Issue: Scanning may be interrupted due to an error during execution of the eXam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...
The Issue: users are not notified of procedure medication discrepancies between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.