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. 1,019 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
1,019 in last 12 months

Showing 17381–17400 of 49,311 recalls

Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.5 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.0 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 2 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Subpotent Drug:...

The Issue: Subpotent Drug: Out-of-Specification potency results at the 30-day stability...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 10 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 29, 2020· Smith Foods Inc.

Recalled Item: Earth Grown brand Mocha Fudge Non-Dairy Frozen Dessert in pint Recalled by...

The Issue: Undeclared cashews in the product.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 29, 2020· Smith Foods Inc.

Recalled Item: Earth Grown brand Vanilla Non-Dairy Frozen Dessert in pint sized Recalled by...

The Issue: Undeclared cashews in the product.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 29, 2020· Smith Foods Inc.

Recalled Item: Earth Grown brand Chocolate Non-Dairy Frozen Dessert in pint sized Recalled...

The Issue: Undeclared cashews in the product.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 28, 2020· Kader Exports Pvt. Ltd.

Recalled Item: Cooked Recalled by Kader Exports Pvt. Ltd. Due to Potential Salmonella...

The Issue: Frozen cooked shrimp is possibly contaminated with Salmonella.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 28, 2020· Wright Medical Technology, Inc.

Recalled Item: Screw Removal Case Assembly Recalled by Wright Medical Technology, Inc. Due...

The Issue: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2020· Wright Medical Technology, Inc.

Recalled Item: Hardware removal kit Recalled by Wright Medical Technology, Inc. Due to...

The Issue: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and...

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

Class II — Potential Health HazardOngoing
DrugJuly 27, 2020· Calvin Scott & Company, Inc.

Recalled Item: Phentermine 15mg grey/Yellow Capsules Recalled by Calvin Scott & Company,...

The Issue: CGMP Deviations: Light sensitive drug products repackaged in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2020· Broncolin, S.A. de C.V.

Recalled Item: HERBACIL Recalled by Broncolin, S.A. de C.V. Due to CGMP Deviations:...

The Issue: CGMP Deviations: products were recalled because they were manufactured in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2020· Calvin Scott & Company, Inc.

Recalled Item: Phendimetrazine Brown/Clear Capsules Recalled by Calvin Scott & Company,...

The Issue: CGMP Deviations: Light sensitive drug products repackaged in...

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

Class II — Potential Health HazardOngoing
Refund