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. 2,423 recalls have been distributed to Idaho in the last 12 months.
Showing 21261–21280 of 27,833 recalls
Recalled Item: P/N: 9735023 Recalled by Medtronic Navigation, Inc. Due to Specific use...
The Issue: Specific use conditions can increase the possibility of a screwdriver tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray systems. Intended to produce...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reverse Shoulder Prosthesis Stem Impaction Fixture The Turon Recalled by...
The Issue: During the assembly, the impaction forces caused the polymer, black acetal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MILEX PESSARY KIT Recalled by CooperSurgical, Inc. Due to The products have...
The Issue: The products have been identified to have incorrect size prints on the MILEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beef Extract Powder Recalled by Acumedia Manufacturers, Inc. Due to...
The Issue: Incorrect expiration date on label. Correct expiration date was March 25,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NicoletOne Software v5.94 Recalled by Natus Neurology Inc Due to When using...
The Issue: When using the NicoletOne v5.94 software, after exiting the impedance check...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAJ-1606 Instrument Channel Adaptor Recalled by Olympus Corporation of the...
The Issue: small puncture marks in a sterile package for an accessory to an Olympus device
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software Anomaly...
The Issue: Software Anomaly during ADD Installation on VITROS 5,1 FS Chemistry Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 8.5 mm Recalled...
The Issue: Sterility of device is compromised due to breach in the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICroSTREP plus 1 Panel Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling MICroSTREP plus 1 and MICroSTREP plus 2 panels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carto 3 EP Navigation System. Electro physiology system which views Recalled...
The Issue: Image disappeared from the cardiac ultrasound system when the CARTO 3 EP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 3.5 mm Recalled...
The Issue: Sterility of device is compromised due to breach in the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOUNDSTAR eco 8F and 10F Diagnostic Ultrasound Catheters. For intra-cardiac...
The Issue: Image disappeared from the cardiac ultrasound system when the CARTO 3 EP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICroSTREP plus 2 Panel Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling MICroSTREP plus 1 and MICroSTREP plus 2 panels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm Recalled...
The Issue: Sterility of device is compromised due to breach in the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 6.5 mm Recalled...
The Issue: Sterility of device is compromised due to breach in the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT i2000SR System The Abbott ARCHITECT System is intended for...
The Issue: Incorrect tubing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluorescence Imaging Procedure Kits used with the da Vinci Si Recalled by...
The Issue: B. Braun 2 gang 4-way stopcocks in the Fluorescence Imaging Procedure Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smooth Muscle Action (SMA) Immunohistochemistry reagent. Catalog numbers:...
The Issue: Certain catalog numbers and lots of Smooth Muscle Actin may stain some cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prism Medical P-300 Portable Consumer Lift Recalled by ErgoSafe Products,...
The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.