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. 2,367 recalls have been distributed to Wyoming in the last 12 months.
Showing 30601–30620 of 48,219 recalls
Recalled Item: Brownwood Farms Jalapeno Cherry Butter. 12oz glass bottles and 1 gallon....
The Issue: Products contain yellow#5 ingredients not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brownwood Farms Jalapeno Cherry Salsa. 21oz glass bottles and 1 Recalled by...
The Issue: Products contain yellow#5 ingredients not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brownwood Farms Peach Salsa. 17oz glass bottles. Private labels: Bowers...
The Issue: Products contain yellow#5 ingredients not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brownwood Farms Cherry BBQ Sauce. 21oz glass bottles Recalled by Brownwood...
The Issue: Products contain soy ingredients not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS 4F Stiffened Micro-Introducer Recalled by Angiodynamics, Inc....
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V6 Rear Case Assembly Recalled by Baxter Healthcare Corp. Due to A...
The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: sigma spectrum VOLUMETRIC INFUSION PUMP with Master Drug Library Recalled by...
The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum INFUSION PUMP with Master Drug Library Recalled by...
The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Gender Solutions" Patellofemoral Joint Prosthesis Milling Handpiece...
The Issue: Complaints have been reported that the handpiece is inoperable. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advance Trauma Kit - Product Code 85-0742 Recalled by North American Rescue...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Range Trauma Kit Hardcase - Product Code 85-0889 Recalled by North American...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Range Trauma Kit ORG - Product Code 80-0213 Recalled by North American...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: USCG Boat Response Kit - Product Code 80-0353 Recalled by North American...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aid Backpack Kit - Product Code 85-0917 Recalled by North American Rescue...
The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.