Product Recalls in New Hampshire

Product recalls affecting New Hampshire — including food, drugs, consumer products, medical devices, and vehicles distributed to New Hampshire. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,747 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
1,747 in last 12 months

Showing 3408134100 of 49,311 recalls

DrugFebruary 16, 2016· Genzyme Corporation

Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...

The Issue: Presence of Particulate Matter: Glass particles found in the product after...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· CareFusion 303, Inc.

Recalled Item: Alaris PC Unit Recalled by CareFusion 303, Inc. Due to CareFusion is...

The Issue: CareFusion is recalling the Alaris PC unit because a component on the PC...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· Biomet Spine, LLC

Recalled Item: 10mm X 12o Solitaire Ti Medium Spacer  Solitaire Anterior Spinal System...

The Issue: Zimmer Biomet Spine initiated a recall of certain Solitaire Ti Spacers...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Helioseal Clear 1 x 1.25 g Recalled by Ivoclar Vivadent, Inc. Due to...

The Issue: Complaints were received claiming the material failed to polymerize under...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Mammomat Inspiration with Tomosynthesis functionality Recalled by Siemens...

The Issue: A potential system fatal error may occur during tomosynthesis reconstruction...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· Zimmer Spine, Inc.

Recalled Item: Instinct¿ Java¿ System (IFU : 046WAN0000T) . Stabilizes one or Recalled by...

The Issue: Zimmer Biomet is initiating a Medical Device Correction Notice to provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· Zimmer Spine, Inc.

Recalled Item: Universal Clamp¿ System (IFU : SNA027-N-90001). Provides the stability...

The Issue: Zimmer Biomet is initiating a Medical Device Correction Notice to provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· Becton Dickinson & Co.

Recalled Item: BD SurePathTM Preservative Collection Vials Recalled by Becton Dickinson &...

The Issue: BD has confirmed that a portion of BD SurePath" collection vials associated...

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

Class II — Potential Health HazardOngoing
FoodFebruary 12, 2016· Wilderness Family Naturals, LLC

Recalled Item: Morning Star Disaster Supplies Creamy Mushroom Wild Rice Soup Recalled by...

The Issue: Wilderness Family Naturals Organic Coconut Milk Powder and other products...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 12, 2016· Faye's Texas Naturals

Recalled Item: Faye's Texas Naturals Chili Petin Picante Muy Caliente Net Wt. Recalled by...

The Issue: pH for the products were not tested and recorded as required by acidified...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 12, 2016· Wilderness Family Naturals, LLC

Recalled Item: Wilderness Family Naturals Coconut Chia Pudding Mix Organic Recalled by...

The Issue: Wilderness Family Naturals Organic Coconut Milk Powder and other products...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 12, 2016· Wilderness Family Naturals, LLC

Recalled Item: Morning Star Disaster Supplies Tomato Basil Soup Recalled by Wilderness...

The Issue: Wilderness Family Naturals Organic Coconut Milk Powder and other products...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund