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. 1,992 recalls have been distributed to Wyoming in the last 12 months.
Showing 7101–7120 of 48,219 recalls
Recalled Item: EZDilate Fixed Wire Balloon 11-12-13. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medex LOGICAL CATH LAB KIT Recalled by Smiths Medical Asd Inc Due to There...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20IN (50.8CM) BRAIDED INJ LINE Recalled by Smiths Medical Asd Inc Due to...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medex 700PSI STOPCOCK W/ROTATOR Recalled by Smiths Medical Asd Inc Due to...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 18-19-20. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 6-7-8. indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 16-17-18. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 13.5-14.5-15.5. Indicated for endoscopic...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 6-7-8. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 18-19-20. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 8.5-9.5-10.5. indicated for endoscopic dilation...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 11-12-13. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 8.5-9.5-10.5. Indicated for endoscopic dilation...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO surgical EMPOWR Porous Knee System Empowr 3D Femur-Porous Coated...
The Issue: Due to incorrect product/device within packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHENYLephrine HCl 40 mg in 0.9% Sodium Chloride Injection Recalled by SCA...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl 1000 mcg/10 mL in 0.9% Sodium Chloride Injection Recalled...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VANCOMYCIN 1.25 g added to 0.9% Sodium Chloride 250 mL Injection Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 2 Recalled by SCA Pharmaceuticals, LLC Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 200 mcg/100 mL Recalled by SCA Pharmaceuticals, LLC 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: SUCcinylcholine Chloride 100 mg/5mL Injection (Concentration = 20mg/mL)...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.