Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,436 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,436 in last 12 months

Showing 2030120320 of 27,833 recalls

Medical DeviceFebruary 8, 2016· Ormco/Sybronendo

Recalled Item: TF Adaptive Gutta Percha Point Size SM3 50pk Recalled by Ormco/Sybronendo...

The Issue: Ormco Corporation is recalling the TF Adaptive Gutta Percha Point Size...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2016· MicroAire Surgical Instruments, LLC

Recalled Item: MicroAire PAL-R4011XL - 40cm x 4 mm Del Vecchio French Rasp aspiration...

The Issue: Complaints that the cannula bent/broke during surgery.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2016· MicroAire Surgical Instruments, LLC

Recalled Item: MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device Recalled by...

The Issue: MicroAire has initiated a recall on product PAL-R4011XL (40cm x 4mm Del...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Volcano Corporation

Recalled Item: Volcano SpinVision Sterile Equip cover II Recalled by Volcano Corporation...

The Issue: Volcano Corporation has identified that certain lot numbers of Volcano R-100...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Beckman Coulter Inc.

Recalled Item: Allegra X-5 rotor yoke Recalled by Beckman Coulter Inc. Due to A defective...

The Issue: A defective rotor yoke on Allegra X-5 allows improper rotor seating on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Volcano Corporation

Recalled Item: Volcano R100 Sterile Equipment Cover Recalled by Volcano Corporation Due to...

The Issue: Volcano Corporation has identified that certain lot numbers of Volcano R-100...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E - 2-Pack Catalog...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: (Stryker) AccuPlace Straight Level Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Draeger Medical, Inc.

Recalled Item: Evita Infinity V500 Ventilator Recalled by Draeger Medical, Inc. Due to The...

The Issue: The battery capacity of the optional PS500 power supply unit for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: (Stryker) AccuPlace Round Level Needle Guide Recalled by Stryker Instruments...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 50000 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Abbott Vascular

Recalled Item: MitraClip Clip Delivery System Recalled by Abbott Vascular Due to Abbott...

The Issue: Abbott Vascular has recently received reports of cases on Clip Delivery...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 50001 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostic ADVIA Centaur Calibrator E- 6- Pack ()...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E- 6- Pack Catalog...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2016· Medical Action Industries Inc

Recalled Item: PICC/CVC Secure Dressing Change kit Recalled by Medical Action Industries...

The Issue: Misbranding; Due to the presence of CHG in the Tegaderm PICC/CVC dressing...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2016· Zimmer Spine, Inc.

Recalled Item: Virage OCT Spinal Fixation System. Intended to promote fusion of Recalled by...

The Issue: Zimmer Biomet Spine is initiating a Medical Device Correction regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: S3 MedSurg Bed Recalled by Stryker Medical Division of Stryker Corporation...

The Issue: CPU board failures cause fowler (backrest) electronic controls to stop working.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2016· Merge Healthcare, Inc.

Recalled Item: Merge OfficePACS software. The firm name on the label is Merge Healthcare...

The Issue: Potential data loss occurs as a result of product archiving not working...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. Product was distributed under the AMICAS label Recalled...

The Issue: The patient name in the Halo title bar and the thumbnails do not match the...

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

Class II — Potential Health HazardOngoing