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. 2,391 recalls have been distributed to Wyoming in the last 12 months.
Showing 23721–23740 of 27,462 recalls
Recalled Item: ADVIA Centaur Systems TSH3 Ultra 2500 tests Catalog Number: 04862625...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems VitD 500 test Recalled by Siemens Healthcare...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes External Fixation Systems (Small Recalled by Synthes, Inc. Due to...
The Issue: Labeling changes have been made related to MR (Magnetic Resonance imaging)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems BRAHMS PCT 100 test Sold only OUS Recalled by Siemens...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation Systems (enGen) with TCAutomation -- For in...
The Issue: Software anomaly: potential for delay in the reporting of patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems TSH3 Ultra Recalled by Siemens Healthcare Diagnostics,...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential for biased results when a Multiple Window (MW) code is associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae Recalled by...
The Issue: Potential for separation of dilator tips.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to When the E-NMT-01 module...
The Issue: When the E-NMT-01 module is used in conjunction with the ElectroSensor, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae with Duraflo...
The Issue: Potential for separation of dilator tips.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cochlear Baha Soft tissue gauge 6mm. Reusable instrument used to Recalled by...
The Issue: Cochlear America is recalling Cochlear Baha Soft Tissue Gauge due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intended for both adult and pediatric patients for taking diagnostic...
The Issue: In special cases, during the start-up of the current model of MobileDiagnost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e.cam -emission computed tomography system Used to detect or image Recalled...
The Issue: There is a potential for patient finger injury on the e.cam systems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Pos Combo Panel Type 33 (PC33): Catalog number B1017-211 Recalled...
The Issue: Siemens investigation confirmed that a portion one lot of panel Pos Combo 33...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)...
The Issue: Separation events have occurred, including the VIPR separating from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipase Reagent Recalled by Abbott Laboratories, Inc Due to Package inserts...
The Issue: Package inserts have incorrect SmartWash parameters for Triglyceride.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SBi RingFix Olive Wires Product Usage: These are temporary devices Recalled...
The Issue: Small Bone Innovations (SBI) is recalling non-sterile RingFIX Olive Wires...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lithium Ion Battery M4605A and M4607A for use with IntelliVue Recalled by...
The Issue: The risk of battery failure increases with age, when a battery remains in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit 8551/856X (includes Models 8561 Recalled by Medtronic Neuromodulation...
The Issue: Some kits in the affected lots may contain an extension tubing set that is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iLab Ultrasound Imaging System Recalled by Boston Scientific Corporation Due...
The Issue: Specific iLab Ultrasound Imaging Systems using newest 3.0 (Polaris 1.0)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.