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. 1,041 recalls have been distributed to Wyoming in the last 12 months.
Showing 12501–12520 of 48,219 recalls
Recalled Item: PHENOBARBITAL Sodium Injection Recalled by Vitae Enim Vitae Scientific, Inc....
The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENOBARBITAL Sodium Injection Recalled by Vitae Enim Vitae Scientific, Inc....
The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine Bitartrate Injection 4mg per 250 mL in 0.9% Sodium Chloride...
The Issue: Defective container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TETRACAINE 1% Tetracaine HCI Injection Recalled by Vitae Enim Vitae...
The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine Bitartrate Injection 8 mg per 250 mL in 0.9% Sodium Chloride...
The Issue: Defective container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epinephrine Injection 8 mg per 250 mL in 0.9% Sodium Chloride Recalled by...
The Issue: Defective container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl Injection 50 mg per 250 mL in 0.9% Sodium Chloride...
The Issue: Defective container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine Bitartrate Injection 16 mg per 250 mL added to Recalled by...
The Issue: Defective container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sucralfate Oral Suspension Recalled by DASH Pharmaceuticals LLC Due to...
The Issue: Labeling: Label Mix-Up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 20/30 Priority Pack w/COPILOT - WPL2122272-01 (2019-03-01) Recalled by...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INDEFLATOR Plus 30 - WPL2122277-01 (2019-03-01) Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plus 30 Priority Pack w/.096 RHV - WPL2122277-01 Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20/30 INDEFLATOR - WPL2122268-01 (2019-03-01) Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20/30 Priority Pack Accessory Kit/.096 RHV - WPL2122270-01 Recalled by...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virus Counter Platform with Model Name VC3100 Recalled by Sartorius...
The Issue: The Virus Counter is an automated laboratory instrument that enables rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VELYS Robotic-Assisted Solution Base Product No.: 451570100 Recalled by...
The Issue: System software v1.5.1 has a system software issue related to the Daylight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q Recalled...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin 2 PCS MER3700 programmer Model MER3400 software Recalled by St. Jude...
The Issue: Due to a programmer software anomaly under very specific circumstance when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS 3650 programmer Model 3330 software Recalled by St. Jude Medical,...
The Issue: Due to a programmer software anomaly under very specific circumstance when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gallant VR Implantable Cardioverter Defibrillator REF # CDVRA500Q Recalled...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.