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. 1,073 recalls have been distributed to Idaho in the last 12 months.
Showing 7461–7480 of 27,833 recalls
Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...
The Issue: An internal technical investigation has confirmed that Thermo Scientific"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...
The Issue: An internal technical investigation has confirmed that Thermo Scientific"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...
The Issue: An internal technical investigation has confirmed that Thermo Scientific"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoreLink LLC Recalled by CoreLink LLC Due to Specific lots of FLXfit...
The Issue: Specific lots of FLXfit implants have internal components that may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000...
The Issue: Warehouse experienced temperature excursions in July and August 2021. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Progressa Bed System Recalled by Baxter Healthcare Corporation Due...
The Issue: The compression links on impacted Progressa beds, listed in Appendix A, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope...
The Issue: Broken Optical fiber cable damage can occur through handling or bending and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam...
The Issue: Broken Optical fiber cable damage can occur through handling or bending and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18239: ASM Omnipod Dash PDM Recalled by Insulet Corporation Due to The firm...
The Issue: The firm has become aware of PDM battery issues, including battery swelling,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GI4000 Electrosurgical Unit - intended to deliver electrosurgical outputs to...
The Issue: Two electronic diode components (D1 & D4) placed in the reverse orientation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium - Visionsense Infrared (IR) Fluorescence Miniature Microscope...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE FIBER...
The Issue: Due to a defect in the outer pouch sterile seal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Laser System Recalled by Spectranetics Corporation Due to Laser...
The Issue: Laser System may detect Error 106 or Error 108 System Failures that will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GentleWave System Posterior CleanFlow Procedure Instrument with Matrices...
The Issue: Procedure Instruments with erroneous unit carton labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extension Tabletop for Operating Table System 1140 Recalled by Getinge Usa...
The Issue: The back rest may unintentionally drop suddenly, resulting in adverse health...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GentleWave System APM Procedure Instrument with Matrix Recalled by Sonendo...
The Issue: Procedure Instruments with erroneous unit carton labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 9 -(GEN) 22 of VITROS Recalled by...
The Issue: Calibration disk Data Release Version (DRV) 6194 to 6200 contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-107: The Phoenix PMIC/ID panel is used for Recalled by...
The Issue: Misformulated minocycline-can cause erroneously increased Minimal Inhibitory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superion¿ Indirect Decompression System (IDS) Model Numbers and Size:...
The Issue: Due to Indirect Decompression System devices exhibiting a potential for weld...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BASIN SET Recalled by American Contract Systems, Inc. Due to Basin Set...
The Issue: Basin Set labeling error: components within the kit are for the Single Basin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.