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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 Apr 30, 2025

BD PYXIS MEDBANK (Name, REF): MEDPASS MODULE, 139088-01; MINI 1FH-1FM, 169-137; MINI 1HH-1FH-1HM, 169-101; MINI…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount

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

Ihb Operations B.v.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

InPen smart insulin pen, REF: MMT-105NNBLNA, MMT-105NNGYNA, MMT-105NNPKNA, MMT-105ELBLNA, MMT-105ELGYNA, MMT105ELPKNA

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0, REF: NIM4CM01; CONSOLE NIM4CM01RF NIM 4.0 REFURBISHED,…

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

Medtronic Xomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

Merit Medical, REF: R2007, EsophyX Z+, (1) Fastener Delivery Device, SterileEO, RxOnly

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

Merit Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

Radiometer ABL90 Series - Radiometer ABL90 FLEX Model Number 393-090 Radiometer ABL90 Series - Radiometer ABL90 FLEX…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Apr 30, 2025

Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007…

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Food

Reported Apr 30, 2025

Apple Juice; clear/translucent bulbous/round glass bottle with white metal screw top lid; (4 - 10 oz bottles per pack;…

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

S Martinelli & Company

FDA (openFDA food enforcement)

Medical devices

Reported Apr 23, 2025

BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196,…

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

Bard Access Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro…

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

Maquet Cardiovascular, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System.

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

Philips North America LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 16, 2025

Cabot Creamery 8oz Extra Creamy Premium Butter, Sea Salted. Packaged as (2) 4oz sticks in cardboard shells; UPC: 0…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Agri-Mark Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 16, 2025

BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex, BD Pyxis" MedBank" MedPass are automated…

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

CareFusion 303, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 16, 2025

Dr. Praeger s California Veggie Fries 8oz,

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

Dr. Praeger's Sensible Foods Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 16, 2025

Lillie's Q Buffalo Wing Sauce. Net wt. 13.5 oz, UPC 810069510972, Case label: Lillie's Q Buffalo Wing Sauce, Item #…

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

Old World Spices & Seasoning, Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 9, 2025

Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a…

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

Nestle-USA, Inc. (Corporate Office)

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 9, 2025

Monterey AL Implant Inserter; 10/12mm; Catalog 48019100.

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

Stryker Spine

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 2, 2025

CVAC Aspiration System, REF: CVC127020-1, and User Manual L00018. Intended for endoscopic examination/treatment of…

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

Calyxo, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 2, 2025

CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital System Model CM3100 -CardioMEMS Backend Web…

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

St. Jude Medical

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2025

BD Pyxis: Anesthesia Station ES, REF: 327, MedStation ES, REF: 323, MedStation ES Tower, REF: 352, CII Safe ES, REF:…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLine H Set & VitaLine H…

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

Oridion Medical 1987 Ltd.

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 19, 2025

CINNABON CLASSIC CINNAMON ROLL INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) 946 mL UPC 0 41271 01993 3…

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

Danone Wave

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 19, 2025

Brand Name: Da Vinci 5 Product Name: ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals Model/Catalog Number: 380730 Software…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 19, 2025

Little Leaf Farms brand Southwest Salad Kit; 7.5 oz, clear plastic clamshell; UPC: 857394006220

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

Little Leaf Farms LLC

FDA (openFDA food enforcement)

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Other states

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.