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. 977 recalls have been distributed to Idaho in the last 12 months.
Showing 28821–28840 of 48,215 recalls
Recalled Item: ECT Internal Fracture Fixation Quick-Connect Drill 2.5 mm Diameter 11 cm...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Bit Jacobs Chuck 1.5 mm Diameter 70 mm Length Recalled by Zimmer...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Femoral Drill 3.7 mm Diameter Replaces...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fracture Fixation Quick-Connect Drill 2.5 mm Diameter 12.5...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Bit Quick-Connect 2.0 mm Diameter 100 mm Length Recalled by Zimmer...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Bit Quick-Connect 3.2 mm Diameter 145 mm Length Recalled by Zimmer...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Periarticular Locking Plate System Drill Standard 2.7 mm Diameter...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fracture Fixation Drill 3.5 mm Diameter (.138 Inch) Recalled by...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Periarticular Locking Plate System Cannulated Drill Standard...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications: out of specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications: out of specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications: out of specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications: out of specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biotech Underground Tri-Ton Hardcore Formula capsules Recalled by DYNAMIC...
The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Discovery Ml X-ray system Recalled by GE Healthcare, LLC Due...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery PET/CT 600 Recalled by GE Healthcare, LLC Due to It...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Hemostasis FDP (Fibrinogen Degradation Products) Assay Kit (30...
The Issue: An issue was discovered with the Pacific Hemostasis Fibrinogen Degradation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Hemostasis FDP Latex Reagent Recalled by Fisher Diagnostics Due to...
The Issue: An issue was discovered with the Pacific Hemostasis Fibrinogen Degradation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery Ml DR X-ray system Recalled by GE Healthcare, LLC...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT660 Recalled by GE Healthcare, LLC Due to It was...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.