Product Recalls in Oklahoma

Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,509 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,509 in last 12 months

Showing 2040120420 of 28,654 recalls

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: 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· 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· 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 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 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 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: 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· 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: 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· 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: 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: 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 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 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
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Hemo software. The firm name on the labeling is Merge Healthcare...

The Issue: Use of the software may show an incorrect value to the user when viewing the...

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 (ICEA) software. The firm name on the Recalled...

The Issue: An error message can occur resulting in the prior studies being unavailable...

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 (ICEA) software. iConnect Enterprise Archive is...

The Issue: The study is archived but cannot be opened in iConnect Access and cannot...

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: Masimo SPO2 Sensor Recalled by Merge Healthcare, Inc. Due to Under certain...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing