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. 2,364 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,364 in last 12 months

Showing 2930129320 of 49,311 recalls

FoodMay 3, 2017· Newly Weds Foods Inc

Recalled Item: B94412 Recalled by Newly Weds Foods Inc Due to Undeclared Milk

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 3, 2017· Newly Weds Foods Inc

Recalled Item: A30040 Recalled by Newly Weds Foods Inc Due to Undeclared Milk

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 3, 2017· Newly Weds Foods Inc

Recalled Item: B22384 Recalled by Newly Weds Foods Inc Due to Undeclared Milk

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 3, 2017· Newly Weds Foods Inc

Recalled Item: B10065 Recalled by Newly Weds Foods Inc Due to Undeclared Milk

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 3, 2017· Newly Weds Foods Inc

Recalled Item: A84249 Recalled by Newly Weds Foods Inc Due to Undeclared Milk

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: SCHRITTMACHER ANGIO X3 Recalled by Medtronic Due to Potential for an...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: CUSTOM SUTURE PACK Recalled by Medtronic Due to Potential for an incomplete...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Cook Inc.

Recalled Item: OptiLite Multi-Use Holmium Laser Fibers Recalled by Cook Inc. Due to Cook...

The Issue: Cook Inc. is initiating a voluntary recall of the OptiLite Multi-Use Holmium...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Sutures. BIOSYN: BIOSYN 4/0 18" VIOLET CV-25 DT Recalled by Medtronic Due to...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Sutures. ENDO STITCH: ENDO STITCH POLYSORB 0 48" U/D DLU SU Recalled by...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Best Practice Kit Recalled by Medtronic Due to Potential for an incomplete...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: USPACK-SUTURE KIT Recalled by Medtronic Due to Potential for an incomplete...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Sutures. MAXON: MAXON 4/0 5X18" GREEN CV-24 D-TACH Recalled by Medtronic Due...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Sutures. POLYSORB: POLSORB 0 18 U/D PRECUT 126R Recalled by Medtronic Due to...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
DrugMay 2, 2017· Lupin Pharmaceuticals Inc.

Recalled Item: Famotidine for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc....

The Issue: CGMP Deviations

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

Class III — Low RiskOngoing
Refund
FoodMay 2, 2017· HVF Inc. d.b.a Huson Valley Farms

Recalled Item: Nutty INFUSIONS Roasted Cashew Butter Recalled by HVF Inc. d.b.a Huson...

The Issue: Listeria monocytogenes contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2017· HVF Inc. d.b.a Huson Valley Farms

Recalled Item: Nutty INFUSIONS Ginger Wasabi Cashew Butter Recalled by HVF Inc. d.b.a Huson...

The Issue: Listeria monocytogenes contamination

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 2, 2017· GE Healthcare, LLC

Recalled Item: Carestation 620 A1 Recalled by GE Healthcare, LLC Due to Carestation 620,...

The Issue: Carestation 620, 650 and 650c has Potential for Elevated FiCO2 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD Recalled by...

The Issue: Implant Direct Sybron Manufacturing is recalling the Legacy Full-Contour...

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

Class II — Potential Health HazardOngoing
DrugMay 1, 2017· Allergan Sales, LLC

Recalled Item: Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic...

The Issue: Failed Impurities/Degradation Specifications: stability testing results did...

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

Class II — Potential Health HazardOngoing
Refund