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. 2,614 recalls have been distributed to Idaho in the last 12 months.
Showing 1421–1440 of 27,833 recalls
Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to KWIK-STIK : 0894P, 0894K and...
The Issue: KWIK-STIK : 0894P, 0894K and LYFO DISK" 0894L may result in failure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold...
The Issue: Device does not comply with the labeling requirements of international...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to KWIK-STIK : 0894P, 0894K and...
The Issue: KWIK-STIK : 0894P, 0894K and LYFO DISK" 0894L may result in failure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Injection needle Recalled by Spiggle & Theis Mt Gmbh Due to Affected product...
The Issue: Affected product show elevated cytotoxicity values. Use of affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UIBC (Unsaturated Iron Binding Capacity) Recalled by Beckman Coulter Inc....
The Issue: Beckman Coulter identified that the Unsaturated Iron Binding Capacity (UIBC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPoint 500 Systems Wash/Waste Cartridge (4 Pack). Material Number:...
The Issue: Siemens Healthcare Diagnostics is recalling the RAPIDPoint 500 Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breathing circuit set Recalled by Hamilton Medical AG Due to Ventilator...
The Issue: Ventilator coaxial breathing circuit may have a crack in blue tubing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 600 Access Immunoassay Analyzer W/Dual Gantry Recalled by Beckman...
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxI 600 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc....
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxI 800 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc....
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 600 Access Immunoassay Analyzer W/Spot B Recalled by Beckman Coulter,...
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 800 Access Immunoassay Analyzer W/Spot B Recalled by Beckman Coulter,...
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 800 Access Immunoassay Analyzer W/Dual Gantry Recalled by Beckman...
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FARAWAVE 1.0 Pulsed Field Ablation Catheter Recalled by Boston Scientific...
The Issue: The potentially impacted units were manufactured using specific equipment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base Recalled...
The Issue: Engaging titanium base was manufactured 180 degrees around the post from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Blood Products Administration Set Dual-Inlet Recalled by Fresenius Kabi...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PILLAR SA Ti Recalled by Orthofix U.S. LLC Due to A 37 mm implant width...
The Issue: A 37 mm implant width intervertebral body fusion device has a labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.