Product Recalls in Idaho
Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,003 recalls have been distributed to Idaho in the last 12 months.
Showing 21401–21420 of 48,215 recalls
Recalled Item: CVS Health Dry Eye Relief Lubricant Eye Drops 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 Preservative Free Lubricant Eye Drops Sensitive Solution Recalled...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nano Tears MXP Forte Clear Emollient Lubricant Gel Drops Twin Pack Recalled...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health Maximum Redness Relief Lubricant Redness Reliever Eye Drops...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Altaire Diclofenac Sodium Opthalmic Solution Recalled by Altaire...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Puralube Petrolatum Ophthalmic Ointment Recalled by Altaire Pharmaceuticals,...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Altaire Ciprofloxacin Ophthalmic Solution 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 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: 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: 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: 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: SNAG FREE SUTURE TRAY Kit Code: SUT14355 - 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: 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: 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: 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: 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: 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: NEONATAL PICC INSERTION TRAY Kit Code: CVI2310 - 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: DRIVELINE MANAGEMENT TRAY Kit Code: DT17780B - 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: 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.