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. 2,383 recalls have been distributed to Wyoming in the last 12 months.
Showing 24161–24180 of 27,462 recalls
Recalled Item: Stiff 25ga Wide Field Endo Illuminator Recalled by Synergetics Inc Due to...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 23ga Chandelier Infusion Cannula Recalled by Synergetics Inc Due to Faulty...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 23ga Mid-Field Endo Illuminator Recalled by Synergetics Inc Due to Faulty...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25ga Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals on the...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 23ga Chow Illuminated Pick Recalled by Synergetics Inc Due to Faulty seals...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC FX 40 instrument Recalled by Becton Dickinson & Co. Due to...
The Issue: Improperly functioning component of a diagnostic medical device may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)...
The Issue: The housing to the Pump's driveline connector became partially or fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium Single Lumen Low-Profile port Recalled by Bard Access Systems Due...
The Issue: Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estrogen Receptor AB-11 (Clone ID5) Mouse Monoclonal Antibody 1 mk Recalled...
The Issue: Reports that the product is not performing as expected. In house testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catheter Recalled by Merit Medical Systems, Inc. Due to Merit Medical...
The Issue: Merit Medical Systems, Inc. is conducting a recall for 3 lots of Maestro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRI Low Profile Single Lumen port with Open-Ended 6.6Fr Silicone Recalled by...
The Issue: Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis Q and Artis Q biplane systems Product Usage: Recalled by...
The Issue: There exists the possibility that during clinical operation, a breakdown of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...
The Issue: Intermittent noise on ECG and/or Respiration waveforms associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8000 and 8015 with Alaris PCA Recalled by CareFusion...
The Issue: CareFusion is recalling the Alaris PC unit (model 8000 and 8015) because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symmetry and CODMAN brands Recalled by Symmetry Medical/SSI Due to The...
The Issue: The Quad-Lock Sterilization Container System may not maintain an effective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Cyclosporine Flex reagent cartridge an in vitro diagnostic...
The Issue: Complaints were received regarding variability in recovery of QC and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Essenta DR Recalled by Philips Medical Systems, Inc. Due to X-ray...
The Issue: X-ray system C-arm casting may loosen and fall
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Update to...
The Issue: Update to correct the possibility for patients or operators to have their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cusa Excel Rx Only CEM" Nosecone for CUSA¿ Excel Recalled by Integra...
The Issue: The blue COAG button on the CUSA Excel CEM nosecone could stick in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Intermittent noise on...
The Issue: Intermittent noise on ECG and/or Respiration waveforms associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.