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. 2,453 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,453 in last 12 months

Showing 1612116140 of 49,311 recalls

Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Covidien ChemoPlus Chemo Spill Kit Recalled by Cardinal Health 200, LLC Due...

The Issue: Gowns included in the kits potentially have rips, holes, tears, incomplete...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Lab Coats SMS 2X-Large White Recalled by Cardinal Health 200, LLC Due to...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Drug Spill Kit-INSTI Recalled by Cardinal Health 200, LLC Due to...

The Issue: Gowns included in the kits potentially have rips, holes, tears, incomplete...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Gown Isolation W/Ties Xl Blue Recalled by Cardinal Health 200, LLC Due to...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing
DrugJanuary 7, 2021· Bausch Health Companies, Inc.

Recalled Item: Phytonadione Tablets 5mg Recalled by Bausch Health Companies, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications:Out of specification during the...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 7, 2021· American Health Packaging

Recalled Item: Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals) Recalled by American...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 7, 2021· Bausch Health Companies, Inc.

Recalled Item: Mephyton (phytonadione) Tablets 5mg Recalled by Bausch Health Companies,...

The Issue: Failed Impurities/Degradation Specifications:Out of specification during the...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 6, 2021· DLC Laboratories, Inc

Recalled Item: Sulfur Ointment 10% Recalled by DLC Laboratories, Inc Due to Labeling: Label...

The Issue: Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 6, 2021· Roche Diagnostics Operations, Inc.

Recalled Item: 9180 Electrolyte Analyzer - Product Usage: intended to be used Recalled by...

The Issue: May display Calcium results on the screen with wrong arrow direction which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2021· Arrow International Inc

Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit 7Fr 3 Lumen- Intended for Recalled by Arrow...

The Issue: The lidstock / information card on the kits correctly states the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2021· Baxter Healthcare Corporation

Recalled Item: Infusion Pump Recalled by Baxter Healthcare Corporation Due to Battery...

The Issue: Battery performance issues related to prolonged storage.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2021· Respironics California, LLC

Recalled Item: PHILIPS BATTERY Recalled by Respironics California, LLC Due to Due to...

The Issue: Due to unqualified "design verification" batteries being shipped to customers.

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

Class II — Potential Health HazardOngoing
FoodJanuary 6, 2021· EVR FOODS INC

Recalled Item: "LAVVA Blueberry Dairy Free Pili Nut Yogurt. NO SUGAR ADDED. Recalled by EVR...

The Issue: Product may contain mold.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 5, 2021· Helena Laboratories, Corp.

Recalled Item: Cascade Abrazo aPTT Test Card - Product Usage: are to Recalled by Helena...

The Issue: Intermittent potential for shorter than expected clot times.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: SD-400U-10 SNAREMASTER PLUS Hot/Cold 10m Recalled by Aomori Olympus Co.,...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Ethicon, Inc.

Recalled Item: Ethicon Dermabond Advanced Topical Skin Adhesive-topical skin adhesive to...

The Issue: Product distributed with a red tape as part of the sterile packaging which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NA-201SX-4021 ASPIRATION NEEDLE VIZISHOT 21G Recalled by Aomori Olympus Co.,...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX LOWER 23G 5MM Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 21G 4MM Recalled by Aomori Olympus Co., Ltd....

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NEEDLEMASTER 4MMx 26G UPPER Recalled by Aomori Olympus Co., Ltd. Due to...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing