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. 1,082 recalls have been distributed to Idaho in the last 12 months.
Showing 5001–5020 of 27,833 recalls
Recalled Item: Vascu-Guard Peripheral Vascular Patch (US) Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Vascular Probe Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Ostene Hemostasis Material Recalled by Baxter Healthcare Corporation...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peri-Guard Repair Patch Recalled by Baxter Healthcare Corporation Due to...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Preveleak Surgical Sealant Recalled by Baxter Healthcare Corporation...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker, Inc. Due to The microcatheter IFU...
The Issue: The microcatheter IFU contains an intended use that has not been evaluated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascu-Guard Peripheral Vascular Patch (GLOBAL) Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter FloSeal Hemostatic Matrix NL Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter FloSeal Hemostatic Matrix RECOTHROM Recalled by Baxter Healthcare...
The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound EA (Ergonomic Advantage) table version Recalled by Oakworks Inc...
The Issue: Backrest platform stress fracture - the table is not operational in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound EA (Ergonomic Advantage) table versions Recalled by Oakworks Inc...
The Issue: Backrest platform stress fracture - the table is not operational in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound EA (Ergonomic Advantage) table versions Recalled by Oakworks Inc...
The Issue: Backrest platform stress fracture - the table is not operational in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu aView 2 A Monitor Recalled by Ambu Inc. Due to Instructions for Use...
The Issue: Instructions for Use have been updated to add the following warning: Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound EA (Ergonomic Advantage) table versions Recalled by Oakworks Inc...
The Issue: Backrest platform stress fracture - the table is not operational in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive SuperPulsed Laser System TFL FIBER CLEAVER Recalled by Olympus...
The Issue: The strippers and cleavers are provided non-sterile and labelled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-5R Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-V2 Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-5 Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-V2R Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-VHR Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.