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 Dec 9, 2020

CAS-930A Flat Panel Monitor (FPD) used in conjunction with the Canon Interventional Angiography System, Model numbers:…

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

Canon Medical System, USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 9, 2020

BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the…

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

Verathon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are…

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

Coloplast Manufacturing US, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 2, 2020

Synergy raw kombucha - Multi-Green; 16 fl. oz. (473 mL) UPC 7 22430 14016 2 GT's Living Foods LLC Beverly Hills, CA

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

GT's Living Foods

FDA (openFDA food enforcement)

Medical devices

Reported Nov 25, 2020

COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns…

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

Merz North America, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 25, 2020

Trader Joe's brand Gluten Free Battered Halibut, SKU 00503822. Product of USA. Frozen product is packed in plastic bag…

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

Orca Bay Foods LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 25, 2020

Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.

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

Thomas Scientific

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2020

SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Product Usage: intended for use in the dermatologic and…

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

Aesthetics Biomedical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2020

EDI Novel Coronavirus COVID-19 IgG ELISA Kit, REF: KT-1032 Per label: This kit is intended for qualitative detection of…

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

Epitope Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2020

Strep B Carrot Broth One-Step, Ref. Z40, UDI: 00819398026499

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

Hardy Diagnostics

FDA (openFDA device enforcement)

Food

Reported Nov 4, 2020

Happy Tot Superfoods Gluten Free Oat Bar Organic Blueberries & Oatmeal. SKU: TB-BLOT-5 and TB-BLOT-5-WM. Ready-to-eat…

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

Nurture Inc. dba Happy Family

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 28, 2020

NanoClave Connector; 1 unit per pouch, 100 multivac pouches per case;UDI (01)10887709051017(17)241201(30)100(10)4549051;…

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

ICU Medical, Inc.

98 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic…

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

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen FIA is a lateral flow immunofluorescent sandwich assay…

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

Quidel Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Genesis (GII) - Product Usage: designed for use in patients in primary and revision surgery, where the posterior…

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

Smith & Nephew, Inc.

40 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Trevo XP ProVue Retriever, REF (Size): 90182 (4MM x 20MM); 90185 (4MM x 30MM); 90186 (6MM x 25MM). Procedure Pack REF:…

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Langston Dual Lumen Catheter

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

Vascular Solutions, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 21, 2020

SwiftHook sold as the following: a. Individually as SwiftHook b. Included with Vega505EE mobile lifts Product Usage:…

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

Handicare AB

FDA (openFDA device enforcement)

Medical devices

Reported Oct 21, 2020

Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Label: LEVO ARM REF 7887-050R MIZUHO OSI -…

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

Mizuho OSI

FDA (openFDA device enforcement)

Food

Reported Oct 21, 2020

Newly Weds Foods G44384 Cinnamon Snack Seasoning X1, 250 lbs. drum

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

Newly Weds Foods Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 14, 2020

SKIPPY Super Chunk Peanut Butter 16.3oz UPC: 00037600110723 packaged in non-flexible plastic container

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

Hormel Foods Corporation

FDA (openFDA food enforcement)

Food

Reported Oct 14, 2020

"Nettle Meadow Artisan Cheese *** Fig Honey Fromage Frais*** Contains pasteurized goat and cows milk*** 5 oz.***"

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

LuMaZu, LLC dba Nettle Meadow

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 7, 2020

365 Whole Foods Market Organic White Cheddar Popcorn, 4 oz. bag, UPC 099482428747, 16 retail units per wholesale case

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

Eagle Family Foods Group LLC

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 7, 2020

Pacific Xtreme (PTCA Balloon Dilation Catheter)

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

ev3 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.