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. 2,598 recalls have been distributed to Idaho in the last 12 months.
Showing 4021–4040 of 48,215 recalls
Recalled Item: Perio Maintenance Rinse 0.63% Stannous Fluoride Concentrated Solution...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Member's Mark Hatch Chile Chicken Enchiladas Recalled by Sam'S Club Due to...
The Issue: Presence of Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CorNeat EverPatch Recalled by CORNEAT VISION, LTD. Due to Retroactive; Due...
The Issue: Retroactive; Due to complaints, labeling correction for permanent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) COMBINED SPINAL AND EPIDURAL...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smaxel Fractional CO2 Laser Recalled by IDS LTD Due to The Smaxel Fractional...
The Issue: The Smaxel Fractional CO2 Laser does not include a Certification label, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET Recalled by...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) PERIPHERAL CONTINUOUS NERVE BL...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) L&D CONTINUOUS EPIDURAL TRAY...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT Recalled by...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE NEXUS 19/20G CATH CONNECTOR Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The connectors may not allow catheters to be inserted as intended if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrobat-i Vacuum Stabilizer System. Model Number C-OM-10000Z Recalled by...
The Issue: Deviations in the manufacturing process created a compromise in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrobat SUV Vacuum Stabilizer System Recalled by Maquet Cardiovascular, LLC...
The Issue: Deviations in the manufacturing process created a compromise in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrobat-i Positioner. Model Number C-XP-5000Z Recalled by Maquet...
The Issue: Deviations in the manufacturing process created a compromise in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter AK 98 Dialysis Machine Recalled by Baxter Healthcare Corporation Due...
The Issue: Baxter is aware of several recalls by other manufacturers related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: (1) Medline Pacer Implant Pack Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Some of the suture packages within the convenience kits contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Medline Open Heart CDS Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Some of the suture packages within the convenience kits contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Shoulder Repair Pack-LF Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Some of the suture packages within the convenience kits contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.