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. 2,576 recalls have been distributed to Idaho in the last 12 months.
Showing 7881–7900 of 27,833 recalls
Recalled Item: SKYN ORIGINAL NON LATEX CONDOM 12CT Recalled by Family Dollar Stores, Llc....
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ Recalled by Family Dollar Stores, Llc....
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) CVS Health Sterile Surgical Pads Recalled by ASO LLC Due to The product...
The Issue: The product falls apart during handling after removal from its primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit...
The Issue: Due to preventative maintenance (PM) not being performed on E-100 generators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene Recalled by Meridian Bioscience Inc Due to When a run is aborted,...
The Issue: When a run is aborted, the cooling period protection does not occur and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CereLink ICP Monitor Recalled by Integra LifeSciences Corp. Due to Integra...
The Issue: Integra has received complaints associated with ICP readings drifting to -50...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Cholesterol- For the quantitative in vitro determination of...
The Issue: Product fails to meet the performance claims quoted on the kit insert:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: etouchus Recalled by Touch US Llc Due to Device was marketed without FDA...
The Issue: Device was marketed without FDA 510(k) clearance or a PMA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit...
The Issue: BD Intraosseous Needle Kits may exhibit: 1) Increased force required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene CDF Nucleic Acid Test Recalled by Luminex Corporation Due to There...
The Issue: There is a potential for false negative results using VERIGENE CDF Stool...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin 2 PCS MER37000 programmer Model MER3400 software Recalled by St. Jude...
The Issue: The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS 3650 programmer Model 3330 software Recalled by St. Jude Medical,...
The Issue: There is a potential for programmer software (Merlin PCS) and remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin.net model MN5000 Software Recalled by St. Jude Medical, Cardiac...
The Issue: The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Enteric Pathogens Nucleic Acid Test Recalled by Luminex Corporation...
The Issue: There is a potential for false negative results using VERIGENE CDF Stool...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethernet cable may be misaligned, the cable jacket (insulation)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nordicBrainEX Recalled by NordicNeuroLab AS Due to When exporting merged...
The Issue: When exporting merged results from the BOLD, DSC, and DCE modules of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethernet cable may be misaligned, the cable jacket (insulation)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARS CoV 2 rapid antigen test kits packaged under the Recalled by North...
The Issue: Various brands of SARS CoV 2 Antigen Rapid Test kits were offered for sale...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.