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. 998 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
998 in last 12 months

Showing 21201–21220 of 48,219 recalls

Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Becton Dickinson & Company

Recalled Item: BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number:...

The Issue: Lot has been confirmed to have no additive within the tube. Sample processed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2019· AtriCure, Inc.

Recalled Item: EPi-Sense Guided Coagulation System with Visitrax Recalled by AtriCure, Inc....

The Issue: The sterile package seal for the Epi-Sense Guided Coagulation System may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2019· Siemens Healthcare Diagnostics Inc

Recalled Item: Stratus CS Acute Care cTNI TestPak Recalled by Siemens Healthcare...

The Issue: Potential for increased rate of false positive results and/or increased rate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2019· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Liberty Cycler Cassettes (a disposable cassette that is intended to Recalled...

The Issue: Additional Instructions: step-by step handling and inserting the cassette...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Zimmer Biomet, Inc.

Recalled Item: DVR Crosslock ePAK Depth Gauge Recalled by Zimmer Biomet, Inc. Due to There...

The Issue: There is a potential for weak seals of the sterile packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229036A...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Up (Model #11061610) with syngo.CT software versions VA20A...

The Issue: The potential sporadic performance problems may result in scanning workflow...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Zimmer Biomet, Inc.

Recalled Item: DVR Crosslock ePAK Screw Driver Recalled by Zimmer Biomet, Inc. Due to There...

The Issue: There is a potential for weak seals of the sterile packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Zimmer Biomet, Inc.

Recalled Item: K-Wire Trochar Tip Recalled by Zimmer Biomet, Inc. Due to There is a...

The Issue: There is a potential for weak seals of the sterile packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.All (Model #11061630) Recalled by Siemens Medical Solutions USA,...

The Issue: The potential sporadic performance problems may result in scanning workflow...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Liquid Gel Radiolucent Recalled by Bio-Detek, Inc. Due to Some...

The Issue: Some of the electrodes may have been assembled incorrectly, preventing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Top (Model #1161640) Recalled by Siemens Medical Solutions USA,...

The Issue: The potential sporadic performance problems may result in scanning workflow...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Now (Model #11061620) Recalled by Siemens Medical Solutions USA,...

The Issue: The potential sporadic performance problems may result in scanning workflow...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229037A Model:...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229003A Model:...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229000A Model:...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568812910 Model:...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229001A Model:...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing