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. 2,552 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,552 in last 12 months

Showing 62016220 of 49,311 recalls

FoodMarch 4, 2024· Natural Waters of Viti Limited

Recalled Item: Fiji Natural Artesian Water 500 mL (24 pack) Case Recalled by Natural Waters...

The Issue: Firm testing revealed Manganese in addition to three bacterial genera.

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2024· Par Sterile Products LLC

Recalled Item: Treprostinil Injection Recalled by Par Sterile Products LLC Due to Presence...

The Issue: Presence of Particulate Matter.

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 4, 2024· Novitium Pharma LLC

Recalled Item: Digoxin Tablets Recalled by Novitium Pharma LLC Due to Cross Contamination...

The Issue: Cross Contamination with Other Products:(mycophenolate mofetil).

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Febuxostat Tablets 80mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Febuxostat Tablets 40mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 4, 2024· Avanos Medical, Inc.

Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...

The Issue: The expiration date was not printed on the outer shipping label, leading to...

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

Class III — Low RiskOngoing
Medical DeviceMarch 4, 2024· Avanos Medical, Inc.

Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...

The Issue: The expiration date was not printed on the outer shipping label, leading to...

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

Class III — Low RiskOngoing
Medical DeviceMarch 4, 2024· Avanos Medical, Inc.

Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...

The Issue: The expiration date was not printed on the outer shipping label, leading to...

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

Class III — Low RiskOngoing
Medical DeviceMarch 4, 2024· Ion Beam Applications S.A.

Recalled Item: IBA Proton Therapy System - PROTEUS 235 Recalled by Ion Beam Applications...

The Issue: There is a risk of mistreatment as irradiation is not prevented when some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· Qiagen Sciences LLC

Recalled Item: EZ2 Connect MDx-IVD Designed to perform automated isolation and purification...

The Issue: Insufficient welding leads to the heater cable becoming brittle and present...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· Abbott GmbH

Recalled Item: ARCHITECT Anti-HCV Reagent Kit Recalled by Abbott GmbH Due to Customer...

The Issue: Customer complaints were received regarding falsely elevated results for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· X-NAV Technologies, LLC

Recalled Item: X-Guide Handpiece Adaptor Sleeve 3 Recalled by X-NAV Technologies, LLC Due...

The Issue: The Handpiece Adaptor may have a manufacturing defect causing incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· X-NAV Technologies, LLC

Recalled Item: X-Guide Handpiece Adaptor Sleeve 1 Recalled by X-NAV Technologies, LLC Due...

The Issue: The Handpiece Adaptor may have a manufacturing defect causing incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· Abbott GmbH

Recalled Item: Alinity i Anti-HCV Reagent Kit Recalled by Abbott GmbH Due to Customer...

The Issue: Customer complaints were received regarding falsely elevated results for...

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

Class II — Potential Health HazardOngoing
DrugMarch 1, 2024· Specialty Process Labs LLC

Recalled Item: S.P Labs Recalled by Specialty Process Labs LLC Due to Failed Stability...

The Issue: Failed Stability Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 1, 2024· Specialty Process Labs LLC

Recalled Item: S.P.Labs Recalled by Specialty Process Labs LLC Due to Failed Stability...

The Issue: Failed Stability Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 1, 2024· PACIFIC LASERTECH, LLC

Recalled Item: 25-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...

The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· PACIFIC LASERTECH, LLC

Recalled Item: N-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...

The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· PACIFIC LASERTECH, LLC

Recalled Item: 25-LHP-828 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...

The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Olympus Corporation of the Americas

Recalled Item: Olympus Triangle Tip Electrosurgical Knives- to be used with Olympus...

The Issue: Due to increase in complaints for the KD-640L and KD-645L Triangle Tip...

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

Class II — Potential Health HazardOngoing