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. 2,404 recalls have been distributed to Wyoming in the last 12 months.
Showing 19721–19740 of 48,219 recalls
Recalled Item: Neocis Guidance System Fiducial Array - Product Usage: The Neocis Recalled...
The Issue: The Fiducial Array may mismatch their measurement files resulting in failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...
The Issue: Device may fail to turn on or unexpectedly attempt to restart, rendering it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX ENDOPATH 60mm Stapler - 340mm shaft Recalled by Ethicon...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 280mm shaft Recalled by...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 340mm shaft Recalled by...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 440mm shaft Recalled by...
The Issue: The staplers may contain an out of specification anvil component within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection Recalled...
The Issue: Lack of Assurance of Sterility: Bag has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Component for Laser Scanning Microscopes (LSM 700 Recalled by Zeiss, Carl...
The Issue: When the user tilts the transmitted light arm of the microscope to the end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4mm x 2.5 Fluted Pin Pouch Recalled by Exactech, Inc. Due to Potential for...
The Issue: Potential for the 2.4mm x 2.5 Fluted Pin Pouch to contain a single pin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCFE (slipped capital femoral epiphysis) Knobs for Driver Recalled by Pega...
The Issue: There is a potential for the screws to have become loosened during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Motion Sickness (meclizine hydrochloride) 25 mg tablets Recalled by Sato...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zentrip (meclizine Hydrochloride) Recalled by Sato Pharmaceutical Inc. Due...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Motion Sickness Strips (meclizine hydrochloride) 25 mg strips Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WAL-DRAM 2 (meclizine Hydrochloride) 25 mg tablets Recalled by Sato...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.