All recall categories

Recalls distributed in New Hampshire

These notices name New Hampshire in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

2,001 stored notices name New Hampshire, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach New Hampshire too — those are in the archive.

Medical devices

Reported Feb 24, 2021

System, X-Ray, Tomography, Computed: Revolution Apex, Revolution CT with Apex Edition

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18S, 1/18 GA Flexcore Biopsy Needle, 1/7F…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Argon Medical Devices, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used in conjunction with passive clip slings is designed…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arjohuntleigh Magog, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Infinity Acute Care System (IACS) Monitoring Solution: The IACS is intended for multi-parameter, physiologic patient…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Draegar Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 17, 2021

"LAVVA Blueberry Dairy Free Pili Nut Yogurt. NO SUGAR ADDED. NET WT 5.3OZ (150g) ***KEEP REFRIGERATED***DISTRIBUTED BY…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Evr Foods Inc.

FDA (openFDA food enforcement)

Food

Reported Feb 17, 2021

Maine Grains Inc. brand Organic Yellow Peas sold between 10/17/2019 and 11/1/2020; product was packaged in 25lb bulk…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Maine Grains, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 10, 2021

FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm, 2.5 mm, 3.0 mm, 3.5 mm, 4.0 mm). Implantable…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 10, 2021

Philips EPIQ Diagnostic Ultrasound System; Model Numbers: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 7G, EPIQ 7C, EPIQ CVx &…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Ultrasound Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 3, 2021

Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Respironics California, LLC

32 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 27, 2021

Penumbra JET 7 Reperfusion Catheter REF 5MAXJET7 The Penumbra JET 7 Reperfusion Catheter with Xtra Flex technology (JET…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Penumbra Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2021

All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G, EPIC 5C, EPIQ 5W, EPIQ 7G, EPIC 7C, EPIQ 7W, EPIQ…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Ultrasound Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

APEX Compounding System Control Panel Module, REF: 601224, Product Code AX1000 - Product Usage: intended for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

B Braun Medical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

MicroScan Pos MIC Panel Type 34 - Product Usage: For the determination of antimicrobial agent susceptibility and/or…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

Flexor Check-Flo Introducer, RPN KCFW-4.0-35-55-RB-HFANL0-HC, Order Number G56229 Flexor Introducers and Guiding…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Cook Inc.

20 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

Viral Transport Medium, 3ml, Ref: R99, Container type: Tube, Packaged: 20 tubes/box, IVD, CVM Transport Media is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hardy Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

42 IN (107 cm) Appx 5.0 ml, 20 Drop Admin Set, Spiros, REF: 20131-01; 31" (79 cm) Admin Set w/20 Drop Integrated Clave…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ICU Medical, Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 23, 2020

Outshine Fruit & Cream Bars - Creamy Pineapple Coconut 6 fruit and dairy bars, 14.7 fl. oz. UPC: 41548 91817 4…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Dreyers Grand Ice Cream, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 23, 2020

Percept PC Implantable Neurostimulator (INS) - Product Usage: The Percept PC is a neurostimulation device for deep…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2020

MAC VU360, Electrocardiograph

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 16, 2020

On the Go Sweet & Salty Trail Mix

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Kanan Enterprises Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 16, 2020

Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Spacelabs Healthcare, Ltd.

FDA (openFDA device enforcement)

Food

Reported Dec 16, 2020

1. Fresh Attitude Baby Spinach, 11 oz. 2. Fresh Attitude Baby Spinach, 5 oz.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Veg Pro International Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 16, 2020

ELI 380 Electrocardiograph - Product Usage: intended to be a high-performance, multichannel resting electrocardiograph.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Welch Allyn, Inc/mortara

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

MX60ET (enhanced enVista Toric) enVista¿ One-Piece Hydrophobic Acrylic Toric Model MX60ET - Product Usage: The lens is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bausch & Lomb Surgical, Inc.

FDA (openFDA device enforcement)

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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.