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. 2,448 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,448 in last 12 months

Showing 1958119600 of 27,462 recalls

Medical DeviceApril 8, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray Systems Product Usage: Intended...

The Issue: The firm became aware of a problem where the system may not map Varian drive...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound imaging system with software version VB10C and...

The Issue: While imaging with a transesophageal (TEE) transducer (Z6Ms, V5Ms, or V7M),...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Computed Tomography X-ray Systems Product Usage: Intended to...

The Issue: The firm became aware of a problem where the system may not map Varian drive...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2016· Limacorporate S.p.A

Recalled Item: SMR glenosphere impactor/extractor Recalled by Limacorporate S.p.A Due to...

The Issue: Complaints of intra-operative breakage of the glenosphere impactors/extractors.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-ray Systems Product Usage: Intended to...

The Issue: The firm became aware of a problem where the system may not map Varian drive...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2016· Merge Healthcare, Inc.

Recalled Item: DR Systems Unity PACS software Recalled by Merge Healthcare, Inc. Due to The...

The Issue: The software is not adding the correct tomo image.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray Systems Recalled by Philips Medical...

The Issue: The firm became aware of a problem where the system may not map Varian drive...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Skytron, Div. The KMW Group, Inc

Recalled Item: EZ Slide Battery/line powered hydraulic table with removable leg section...

The Issue: The potential exists within the identified tables that incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Ortho Clinical Diagnostics confirmed a software timing anomaly in which the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Signmoidoscope Product Usage: Intended to provide optical visualization of...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Confocal GI Scope Product Usage: Intended to provide optical visualization...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Duodenoscope Product Usage: Intended to provide optical visualization of and...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Gastroscope Product Usage: Intended to provide optical visualization of and...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Ultrasound Gastroscope Product Usage: Intended to provide optical...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Colonoscope Product Usage: Intended to provide optical visualization of and...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics confirmed a software timing anomaly in which the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2016· Ceg Enterprises Llc

Recalled Item: Germ Terminator Recalled by Ceg Enterprises Llc Due to CEG Enterprises, LLC...

The Issue: CEG Enterprises, LLC is recalling Germ Terminator Toothbrush Sanitizer GT100...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Hemo software. Product Usage: Merge Hemo is a hemodynamic Recalled by...

The Issue: In some instances, the system will lock tabs within a study, even when a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive when used with RadSuite. The firm name Recalled...

The Issue: The software produced a number of "do not route" exceptions, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station Import Utility (ESIU). The firm name on Recalled by Merge...

The Issue: System locks up which may result in potential patient injury or delay in...

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

Class II — Potential Health HazardOngoing