Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,535 recalls have been distributed to Wyoming in the last 12 months.
Showing 7241–7260 of 48,219 recalls
Recalled Item: INDICAID COVID-19 Rapid Antigen At-Home Test Recalled by PHASE SCIENTIFIC...
The Issue: COVID-19 rapid antigen at home tests were released with an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD11b APC: ASR Recalled by Becton, Dickinson and Company, BD Biosciences Due...
The Issue: In vitro diagnostics product that impacts the quality of cell staining can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) Recalled by...
The Issue: Use of a 1.4 drill in hard bone conditions caused increased insertion forces...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products ECO2 Slides-For in vitro diagnostic use only....
The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed during routine testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GRAPHENANO DENTAL G-CAM Recalled by GRAPHENANO DENTAL SL Due to Machining...
The Issue: Machining error on cams renders the device unusable.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liberty Select Cycler Recalled by Fresenius Medical Care Holdings, Inc. Due...
The Issue: Affected Liberty Select cyclers may display an incorrect time stamp on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phenytoin Oral Suspension Recalled by The Harvard Drug Group LLC dba Major...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules Recalled by Glenmark...
The Issue: Failed Impurities/Degradation Specifications:Out of Specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ranolazine Extended-Release Tablets 500mg Recalled by Glenmark...
The Issue: Failed Dissolution Specifications: Out of specification for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX Recalled by Philips North America Llc Due to Potential...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Initial System Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Power/Pulsar Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Recalled by Philips North America Llc Due to Potential component...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artri King con Origa y Omega 3 tablets Recalled by Botanical Be Due to...
The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bisoprolol Fumarate and Hydrochlorothiazide Tablets Recalled by Glenmark...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Reumo Flex caplets Recalled by Botanical Be Due to Undeclared Diclofenac
The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kuka Flex Forte caplets Recalled by Botanical Be Due to Undeclared Diclofenac
The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.