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 24141–24160 of 55,896 recalls
Recalled Item: CVS Health Lubricant Eye Drops for Mild to Moderate Dry Eye Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health Lubricant Eye Drops Multi-Symptom Eye Relief Recalled by Altaire...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Equate Support Advanced Twin Pack W-M item #: 567371433 Recalled by Altaire...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health Fast Acting Lubricant Eye Drops Dry Eye Therapy Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health Redness Relief Lubricant Redness Reliever Eye Drops Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ActivEyes Altachlore Solution Recalled by Altaire Pharmaceuticals, Inc. Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OCuSOFT retaine NaCl Ophthalmic Ointment Recalled by Altaire...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: daVinci XI Sureform 60 reload Recalled by Intuitive Surgical, Inc. Due to...
The Issue: The firm became aware of a manufacturing variation in which black and green...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LACERATION TRAY Kit Code: SUT18370 - Product Usage: Kit is Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch EasyCath Kit Recalled by Teleflex Medical Due to Potential for product...
The Issue: Potential for product not to be sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Sexual Health Testing Kit Recalled by Privapath Diagnostics Ltd...
The Issue: A supplier informed PrivaPath Diagnostics that there is a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVAD DRESSING SYSTEM W/BIOPATCHKit Code: DM700 - Product Usage: Kit Recalled...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE GRAVES VAGINAL SPECULUM MEDIUM Kit Code # GVS10MST - Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIRCUMCISION TRAY Kit Code: CIT2245 - Product Usage: Kit is Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DAILY DRIVELINE KIT Kit Code: DM940 - Product Usage: Kit Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRIVELINE MANAGEMENT SYSTEM 1 DAILY Kit Code: DT18440A - Product Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Erisma- LP posterior fixation system with the below specifically affected...
The Issue: Potential for the polyaxial screw to become disassembled during implant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: daVinci XI Sureform 60 Reload Recalled by Intuitive Surgical, Inc. Due to...
The Issue: The firm became aware of a manufacturing variation in which black and green...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIGH DRAINAGE LVAD TRAY Kit Code: DM950 - Product Usage: Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIRCUMCISION TRAY Kit Code: CIT2650H - Product Usage: Kit is Recalled by...
The Issue: Potential for sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.