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.

2,034 stored notices name New Hampshire, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach New Hampshire too — those are in the archive.

Medical devices

Reported Dec 31, 2025

BECKMAN COULTER BICARBONATE REF: OSR6137 OSR6237 OSR6637 OSR6x37 Bicarbonate is a system reagent for the quantitative…

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

Beckman Coulter Ireland, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 31, 2025

BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324, BD Pyxis MedStation ES Tower,…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 31, 2025

da Vinci 5, Surgeon Console Column Motor Connector; ASSY,DV5 CONSOLE,SSC,IS5000; Part Number: 380730-40

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2025

Alinity ci-series System Control Module (SCM), REF: 03R70-01, 03R70-20

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

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2025

Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10

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

Cepheid

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2025

1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum transfer device, for WASP* *Compatible with…

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

Copan Italia

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2025

Intelerad InteleShare software, with ProViewer component

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

DICOM Grid, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2025

InPen App, Model/CFN Number: MMT-8061 (Android Users)

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2025

Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-12-PK…

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

Rocket Medical PLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2025

Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer System Model/Catalog Number:…

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

Orthofix U.S. LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2025

AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The AMSCO 7052HP Washer/Disinfector…

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

Steris Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 10, 2025

Costco Item# 19927 Kirkland Signature Caesar Salad, refrigerated, packaged in clear plastic clamshell container. The…

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

Costco Wholesale Corporation

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 10, 2025

Genepro Whey 4th Generation Plasma Treated Protein, unflavored, Net Wt. 225g, 30 servings, packaged in a resealable…

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

Genepro Protein, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 10, 2025

Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,

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

Philips Ultrasound, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 10, 2025

Italian Salad Dressing; Net 1 GAL (3.78L) SKU: 7 67367 00518 4 Creamy Poblano Avocado Ranch Dressing and Dip; Net…

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

Ventura Foods LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2025

CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/…

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

Alcon Research LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated…

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

Argon Medical Devices, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

BioFire Respiratory Panel 2.1, IVD, REF: 423742 (30 test kit)

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 3, 2025

Jeni's Passion Fruit Dreamsicle Ice Cream Bars, 3 FL OZ (89 ML)/9 FL OZ (266 ML), packaged 3 bars per retail carton…

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

Jeni's Splendid Ice Creams LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2025

CareLink Clinic, REF: MMT-7350

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 3, 2025

Nat's Nuts Cinnamon Whiskey Pecans, 4 oz.

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

Nats Nuts LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 26, 2025

REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer DI-60, IVD in conjunction with a Honeywell Vuquest…

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

Cellavision AB

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

Meridian Bioscience, alethia c. Difficile, Catalog Number 480050, Nucleic Acid Amplification Test Assay

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

Meridian Bioscience Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

PhD Hemostasis Valve, REF: IN4802/K, IN4802/T, IN4918/A, IN7802/C, IN8802/C, IN9802, IN9802/A, K05-02166B, K05T-02138A,…

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

Merit Medical Systems, Inc.

FDA (openFDA device 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.