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. 2,576 recalls have been distributed to Idaho in the last 12 months.
Showing 7761–7780 of 27,833 recalls
Recalled Item: NARMD MEDICAL DEPOT Scissors Iris Curved 4.5" Recalled by Stradis Medical,...
The Issue: The sterile barrier may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin METAFIX HIP STEM Recalled by Corin Ltd Due to One MetaFix size 7...
The Issue: One MetaFix size 7 collarless stem from batch 478179 which was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TANDEM LIFE LivaNova LIFESPARC Controller Recalled by Cardiac Assist, Inc...
The Issue: Critical Failure of the LifeSPARC controller when the software freezes or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline CHEST TUBE REORDER NO: DYNJ36762A Recalled by Medline Industries...
The Issue: Due to a non-sterile component (tape) being place within the sterile portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-air Ventilator System-The Servo-air Ventilator System is: Intended for...
The Issue: Device does not meet regulatory requirements of stability while stationary,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iSED Primary Pump Tubing Spare Part Kit- (IVD) tubing is Recalled by Alcor...
The Issue: Primary Pump Tubing Spare Part is incorrect. If the tubing is installed onto...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Bronchovideoscope Recalled by Aizu Olympus Co., Ltd. Due to...
The Issue: The recalled unit was utilized in a veterinary endoscopy procedure in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Critical Care AB/Getinge Servo-u Ventilator System Recalled by...
The Issue: Ventilators may generate a combination of alarms which may result in loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NuVasive MD Pulse III Multimodality System Pulse Software Recalled by...
The Issue: Due to an incorrect security key, customers were unable to connect to remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.