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. 1,677 recalls have been distributed to Wyoming in the last 12 months.
Showing 46281–46300 of 48,219 recalls
Recalled Item: Glycerin 100% PF Recalled by New England Compounding Center Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylprednisolone Acetate 40 mg/mL Injection Recalled by New England...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isovue 200 mg/mL PF and 300 mg/mL PF Recalled by New England Compounding...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Omnipaque 240mg/mL PF Recalled by New England Compounding Center Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Saline 10% and 3% Recalled by New England Compounding Center Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone 10 mg/mL P Recalled by New England Compounding Center Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine 1% PF Recalled by New England Compounding Center Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betamethasone Repository 6 mg/mL PF Injection and Betamethasone Repository 6...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betamethasone Sodium Phosphate 6 mg/mL P Injection Recalled by New England...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bupivacaine 0.25% PF Recalled by New England Compounding Center Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylprednisolone Acetate (PF) 80 mg/ml Injection Recalled by New England...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonidine 100 mcg/mL PF Recalled by New England Compounding Center Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine/Dextrose 5%/7.5% PF Recalled by New England Compounding Center Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone Sodium Phosphate 4 mg/mL vials PF Recalled by New England...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hyaluronidase 150 u/ml PF Recalled by New England Compounding Center Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moon Pie(R) Crunch Peanut Butter Recalled by Chattanooga Bakery Inc Due to...
The Issue: Peanut Butter Crunch Moon Pies were manufactured with peanut butter supplied...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (l) Visum Halogen Surgical Light Recalled by Stryker Communications, Inc....
The Issue: Stryker has become aware that there is a low likelihood of incomplete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.