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. 2,278 recalls have been distributed to Wyoming in the last 12 months.
Showing 48201–48219 of 48,219 recalls
Recalled Item: Finger Sensor for Remmers Recorder (Formerly SnoreSat Sleep recorder) To...
The Issue: The outer jacket is receding away from the black sensor prematurely.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI PET/CT System Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: The reason for this inspection is to determine if the Spindle Block Servo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PT Link Waterbath Recalled by Dako North America Inc. Due to Dako is...
The Issue: Dako is recalling the PT Link Waterbath because of a possible electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba CT systems Recalled by Toshiba American Medical Systems Inc Due to...
The Issue: The systems all have a similar table control board. It has been found that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics...
The Issue: The power to the Esprit Display's Backlight is interrupted, causing the GUI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HiRes 90K devices with Helix Electrodes Model CI 1400-02H The Recalled by...
The Issue: Advanced Bionics is recalling the the HiRes 90K cochlear implant with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leflunomide tablets Recalled by Apotex Corp. Due to Subpotent (Single...
The Issue: Subpotent (Single Ingredient Drug): Distribution of product that did not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leflunomide tablets Recalled by Apotex Corp. Due to Subpotent (Single...
The Issue: Subpotent (Single Ingredient Drug): Distribution of product that did not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OEC MiniView 6800 Mobile Recalled by GE OEC Medical Systems, Inc Due to...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroView 2800 Recalled by GE OEC Medical Systems, Inc Due to Please be aware...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9800 Plus Digital Recalled by GE OEC Medical Systems, Inc Due to Please...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cannulaide Recalled by Beevers Manufacturing & Supply, Inc. Due to...
The Issue: Cannulaide model CA 101 was recalled because the firm discovered this model...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PT113950 PT HYBRID Glenoid Post Regenerex porous titanium construct Sterile...
The Issue: Biomet is recalling Part Number PT-113950 PT Hybrid Glenoid Post, following...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 8800 Flexview Recalled by GE OEC Medical Systems, Inc Due to Please be...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC InstaTrak 3500 Recalled by GE OEC Medical Systems, Inc Due to GE...
The Issue: GE Healthcare had recalled certain OEC InstaTrak 3500 Carts due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InstaTrak with Multiple Dataset Navigation Recalled by GE OEC Medical...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUN|DASH RADIUS 252 tanning system Recalled by JK Products & Services, Inc...
The Issue: The firm has tracked a systematic failure in the door cord on the Sun|Dash...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Prisma 2K Hearing Aid Product Usage: A behind the Recalled by...
The Issue: Siemens became aware of an issue where an infant or child could open the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knorr Pasta Sides Cheesy Bacon Macaroni Net Wt. 3.8 oz Recalled by Unilever...
The Issue: Knorr Pasta Sides Cheesy Bacon Macaroni may contain soy as a different...
Recommended Action: Do not consume. Return to store for a refund or discard.