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. 2,540 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,540 in last 12 months

Showing 81818200 of 49,311 recalls

DrugJuly 14, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: CARDIOPLEGIA SOLUTION Recalled by Central Admixture Pharmacy Services, Inc....

The Issue: Lack of assurance of sterility. Validation data for decontamination cycles...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: vancomycin 1.25 g/250 mL added to 0.9% Sodium Chloride Recalled by Central...

The Issue: Lack of assurance of sterility. Validation data for decontamination cycles...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: CARDIOPLEGIA SOLUTION Recalled by Central Admixture Pharmacy Services, Inc....

The Issue: Lack of assurance of sterility. Validation data for decontamination cycles...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 14, 2023· Ozona Organics LLC

Recalled Item: OZONA ORGANICS LIQUID PROBIOTICS & GO HEALTHY LIQUID PROBIOTICS Recalled by...

The Issue: Products contain high water activity in the formula that provides a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 14, 2023· ONO LLC

Recalled Item: ONO Vegan Blueberry Muffin Protein Overnight Oats Recalled by ONO LLC Due to...

The Issue: Undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 14, 2023· Peter Lazic Gmbh

Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...

The Issue: Wrong product coloring. The paddle clips should be blank, but they are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2023· Peter Lazic Gmbh

Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...

The Issue: Wrong product coloring. The paddle clips should be blank, but they are...

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

Class II — Potential Health HazardOngoing
DrugJuly 13, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Methylphenidate Hydrochloride Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Presence of Foreign Substance: Metal embedded in a tablet.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 13, 2023· New Vitalis Pharmacy LLC dba New Vitalis Pharmacy

Recalled Item: Testosterone Cypionate-Testosterone Propionate 180-20 mg/mL in cottonseed...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 13, 2023· EMPATICA SRL

Recalled Item: Embrace2- Indicated for use as an adjunct to seizure monitoring Recalled by...

The Issue: May have a battery life lasting less than the full 48 hours, requiring the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2023· Instrumentation Laboratory

Recalled Item: ACL TOP Family 50 Series Models as follows: In vitro Recalled by...

The Issue: Sample misidentification could occur under specific conditions and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2023· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Redwood 2.0 ultrasound systems Recalled by Siemens Medical Solutions...

The Issue: If a user-generated preset for an 18L6 transducer created on a 1.0...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Olympus Corporation of the Americas

Recalled Item: The Air/Water Valve is provided/used with the following Endoscopes:...

The Issue: The air/water valve MAJ-1444 used with OER-Pro and OER-Elite may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX S Recalled by Medicrea International Due to There is a potential for a...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX C+ Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX MANTA Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Draeger Medical, Inc.

Recalled Item: Carina Sub-Acute Care Ventilator Recalled by Draeger Medical, Inc. Due to...

The Issue: Presence of polyether polyurethane (PE-PUR) and emission of...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX ALIF Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: GRANVIA-C Recalled by Medicrea International Due to There is a potential for...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2023· Medicrea International

Recalled Item: IMPIX MANTA+ Recalled by Medicrea International Due to There is a potential...

The Issue: There is a potential for a product packaging non-conformity issue which...

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

Class II — Potential Health HazardOngoing