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. 2,510 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,510 in last 12 months

Showing 1332113340 of 27,462 recalls

Medical DeviceJune 5, 2019· GETINGE US SALES LLC

Recalled Item: PulsioFlex Monitoring System Recalled by GETINGE US SALES LLC Due to The...

The Issue: The monitor displays an error message . The error message states "internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2019· Inlightened Partners LLC

Recalled Item: inLight Medical LED Pads used with Polychromatic light technology system...

The Issue: LED pads with cord connectors that have v-shaped notches may not have been...

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

Class III — Low RiskOngoing
Medical DeviceJune 4, 2019· Zimmer Biomet, Inc.

Recalled Item: Ultra-Drive Irrigation Tubing Assembly Recalled by Zimmer Biomet, Inc. Due...

The Issue: The products do not have sufficient data to support the labeled shelf life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2019· Zimmer Biomet, Inc.

Recalled Item: Ultra-Drive Hose/Drape Assembly Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The products do not have sufficient data to support the labeled shelf life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The potential sporadic performance problems may cause scanning workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The potential sporadic performance problems may cause scanning workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The potential sporadic performance problems may cause scanning workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.All Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The potential sporadic performance problems may cause scanning workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Vereos PET/CT Recalled by Philips Medical Systems (Cleveland) Inc Due to The...

The Issue: The Vereos PET/CT may have misaligned front and rear covers, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion DIFFICULT IV KIT containing BD's Vacutainer Plastic Lithium...

The Issue: False elevation of carboxyhemoglobin (COHb) results in blood samples...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM XK Alphacurve Long-Term Hemodialysis Catheter REF/Product...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter Recalled by Bard Peripheral...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing