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. 1,997 recalls have been distributed to Wyoming in the last 12 months.
Showing 6201–6220 of 48,219 recalls
Recalled Item: Trocar Needle - Used for dilating puncture sites or catheter Recalled by...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti HBs Calibrators. The VITROS Anti-HBs...
The Issue: Potential for positively biased results due to signal reduction over shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dilator - Coons Taper - Used for dilating puncture sites Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dilator With AQ Hydrophilic Coating - Intended to be used Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chiba Biopsy Needle - Used for aspiration biopsy. PART Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo 2 Full Face AAV Non Vented Mask Recalled by SleepNet Corporation Due to...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iQ 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update to...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peel-Away Introducer - Intended for the percutaneous introduction of balloon...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Trumpet Needle Guide ring can detach when excessive pressure is applied.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo Full Face with Headgear Recalled by SleepNet Corporation Due to Update...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phantom 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo 2 Full Face Non Vented Mask Recalled by SleepNet Corporation Due to...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion OB INSTRUMENT TRAY Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Trumpet Needle Guide ring can detach when excessive pressure is applied.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo Non Vented Full Face Mask with Headgear Recalled by SleepNet...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate 3 Recalled by Thoratec Corp. Due to Potential for a leak...
The Issue: Potential for a leak path at the seal interface between the left ventricle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S.P.Labs Recalled by Specialty Process Labs LLC Due to Failed Stability...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: S.P Labs Recalled by Specialty Process Labs LLC Due to Failed Stability...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 25-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25-LHP-828 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.