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. 2,498 recalls have been distributed to Idaho in the last 12 months.
Showing 16081–16100 of 27,833 recalls
Recalled Item: Smooth Guide Wire Bullet Tip 3.0 mm Diameter Recalled by Zimmer Biomet, Inc....
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...
The Issue: Use of the product with insufficient lubrication may prolong surgery due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnostic-Eleva with Flat Detector 708035 As a multifunctional...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mutlidiagnost-Eleva with Flat Detector Eleva with Flat Detector 708037 As...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BECKMAN COULTER MicroScan MICroSTREP Plus Panel Recalled by Beckman Coulter...
The Issue: Beckman Coulter has received customer complaints of lowered minimum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire 2.4 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 0.15 ml 5-Pack. Enamel Matrix Derivative. Article Number...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 015 Recalled by Straumann Manufacturing, Inc. Due to A...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 0.7 ml Multipack. Enamel Matrix Derivative. Article...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 0.3 ml Multipack. Enamel Matrix Derivative. Article...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 0.3 ml Multipack USA. Enamel Matrix Derivative. Article...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visualase Cooled Laser Applicator System (VCLAS) labeled as: a. Part...
The Issue: Medtronic has become aware that certain lots of the VCLAS 3MM, 10MM, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic ZEVO(TM) Anterior Cervical Plate System SLOT SCREW Recalled by...
The Issue: Slot screw had an overall length of 15mm, but per the specification, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 0.7 ml Multipack USA. Enamel Matrix Derivative. Article...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE LOGIQ E9 ultrasound system Product Usage: The device is Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Lithium Heparin Green Top Tube Recalled by Becton Dickinson &...
The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.