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. 2,544 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,544 in last 12 months

Showing 1334113360 of 27,833 recalls

Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 20 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 30 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 40 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 20 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 30 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Heidelberg Engineering GmbH

Recalled Item: SPECTRALIS with HEYEX2 image management system. a non-contact ophthalmic...

The Issue: Error in the default configuration which could lead to the incorrect display...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Drive Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Edge Plus Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Confidence Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: CoolBlue Hyper-Hypothermia System- body hypothermia system Model: Innercool...

The Issue: Warnings statements have been added- exceeding 40 degree C for extended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Blanketrol III Hyper-Hypothermia System- body hypothermia system temperature...

The Issue: Warnings statements have been added- exceeding 40 degree C for extended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Blanketrol II Hyper-Hypothermia System Recalled by Cincinnati Sub-Zero...

The Issue: Warnings statements have been added- exceeding 40 degree C for extended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: The Tina-Quant Myoglobin Gen. 2 Tests system is an immuno-turbidimetric...

The Issue: The firm conducted internal investigations that confirmed customer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Qiagen Sciences LLC

Recalled Item: QIAsymphony SP SOW 5.0.3 Recalled by Qiagen Sciences LLC Due to QIAsymphony...

The Issue: QIAsymphony software version 5.0.3 - Software issue incorreclty assigns the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Intuitive Surgical, Inc.

Recalled Item: daVinci XI Sureform 60 Reload Recalled by Intuitive Surgical, Inc. Due to...

The Issue: The firm became aware of a manufacturing variation in which black and green...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2019· Intuitive Surgical, Inc.

Recalled Item: daVinci XI Sureform 60 reload Recalled by Intuitive Surgical, Inc. Due to...

The Issue: The firm became aware of a manufacturing variation in which black and green...

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

Class II — Potential Health HazardOngoing