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 21161–21180 of 27,462 recalls
Recalled Item: Medtronic Passive Biopsy Needle Kit Recalled by Medtronic Navigation, Inc....
The Issue: The adhesive between the sphere assembly and the biopsy needle shaft may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Passive Biopsy Needle Kit Recalled by Medtronic Navigation, Inc....
The Issue: The adhesive between the sphere assembly and the biopsy needle shaft may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO Disk Recalled by Microbiologics Inc Due to LYFO Disk Catalog #0983L is...
The Issue: LYFO Disk Catalog #0983L is to contain Candida tropicalis. However, lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Robotic Arm Interactive Orthopedic (RIO) system component PN#205143 (locking...
The Issue: The locking pin on the RIO Base Array is damaged during assembly onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ottobock Pheon 3R62 Knee Joint The 3R62 Pheon is a Recalled by Otto Bock...
The Issue: Otto Bock Healthcare GmbH is voluntarily recalling all 3R62 Pheon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Naturalyte Liquid Bicarbonate Concentrate 6.4 liter bottle A Dialysate...
The Issue: Expansion of recall to lots manufactured in 2015 due to the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 Ventilator System Recalled by Covidien LP (formerly...
The Issue: Reports in which tidal volumes reaching patients were lower than set tidal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnVeo R Loading System Recalled by Medtronic Cardiovascular Surgery-the...
The Issue: Medtronic is recalling the EnVeo R Loading Systems because of the presence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iChemVELOCITY Automated Urine Chemistry Catalog No. 800-3049 Recalled by...
The Issue: Iris International is recalling the iChemVELOCITY systems because they do...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension¿ CREA (Creatinine) and Dimension Vista¿ CREA (Creatinine) Recalled...
The Issue: Siemens has confirmed that the Dimension CREA and Dimension Vista CREA may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas b 123 Fluid Pack COOX 400 Product Recalled by Roche Diagnostics...
The Issue: Low PO2 results. QC failures of the PO2 parameter, affecting primarily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas b 123 Fluid Pack COOX 200 Product Recalled by Roche Diagnostics...
The Issue: Low PO2 results. QC failures of the PO2 parameter, affecting primarily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadPro 40kW Digital X-Ray Panel and Mobile/Portable Diagnostic X-Ray....
The Issue: Electrostatic energy may be stored in Systems that can cause a short-cicuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected....
The Issue: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected....
The Issue: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS500 of an IACS Workstation Critical Care (Evita Infinity V500) Recalled by...
The Issue: The battery capacity of the optional PS500 of an IACS Workstation Critical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etac Relax wall mounted shower seat The Etac Relax is Recalled by Etac...
The Issue: The recalling firm has received reports of a malfunction of the Relax wall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to A gradient cable in the ACGD...
The Issue: A gradient cable in the ACGD cabinet may be missing a spacer that prevents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Sustainability Solutions CB5LT Ethicon Endo-Surgery Recalled by...
The Issue: Stryker Sustainability Solutions has received reports indicating that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro-Mate Tuberculin Glass Syringe Recalled by Cadence Inc. Due to...
The Issue: Graduation marks of the syringe are not centered with the numeric position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.