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 Aug 1, 2018

Arctic Sun Temperature Management System, Model 5000. The Arctic Sun¿ 5000 model is a non-invasive, thermal regulating…

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

Bard Medical Division

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

CORAIL Cementless Femoral Stem HA Coated Standard Size 11, Catalog No. 3L92511

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

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2018

Dimension Vista¿ CTNI Sample Diluent, KD692, SMN# 10445205

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

Siemens Healthcare Diagnostics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 18, 2018

BioMerieux mini VIDAS System in combination with Quality Control VIDAS* (QCV*) Product Usage: the Quality Control VIDAS…

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

bioMerieux, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 18, 2018

PD-L1 IHC 22C3 pharmDx is a companion diagnostic used to determine PD-L1 levels for determination of patient treatment…

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

Dako North America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 18, 2018

Discovery IGS 730 Interventional Fluoroscopic X-ray Systems

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

GE Medical Systems, SCS

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 11, 2018

microTargeting" Drive System, Product Number MT-DS

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

FHC, Inc.

14 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 11, 2018

Icelandic Provisions Vanilla Skyr cups, 5.3oz package, UPC: 854074006068

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

Icelandic Provisions Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 11, 2018

St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor, Sterile EO, Model #: DM3500 The Confirm Rx ICM is indicated for…

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

St Jude Medical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 4, 2018

Single Chamber Temporary External Pacemaker, Model 53401

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

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

FDA (openFDA device enforcement)

Food

Reported Jul 4, 2018

Utz Restaurant Style Tortilla Chips; Net Wt 17 oz; White Corn Tortilla Chips; UPC: 0-41780-00383-6; Exp. Date Jun 16…

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

Utz Quality Food Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 27, 2018

Fabius GS Premium Anesthesia Machine; Cat. no. 8607000 Product Usage: Inhalation anesthesia machines for use in…

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

Draeger Medical, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 27, 2018

Kellogg's Honey Smacks, 15.3 oz. and 23 oz.

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

Kellogg Company

FDA (openFDA food enforcement)

Food

Reported Jun 20, 2018

Snak Club Tropical Trail Mix: 16 oz. plastic pouch: Ingredients: Raisins, Peanuts, Pineapple, Papaya, Banana Chips,…

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

New Century Snacks LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 20, 2018

IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865350

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

Philips Electronics North America Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 13, 2018

Priano Rosso Pesto Sauce, 6.7oz glass jar

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

BLM Products U. Vertriebsges

FDA (openFDA food enforcement)

Medical devices

Reported Jun 13, 2018

Draeger Jaundice Meter JM-103 The device is intended for use in hospitals, clinics or doctor s offices under a…

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

Draeger Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity PACS-IW with Universal Viewer is a device…

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

GE Healthcare

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio physiomonitoring system is used to facilitate invasive…

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

Invivo Corporation

FDA (openFDA device enforcement)

Food

Reported Jun 13, 2018

Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, Multiple sizes: 8 oz, 16 oz, 32 oz, 64 oz, 1 gal, 2.5 gals, 5…

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

Lake Michigan Distilling Co. LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 13, 2018

Restoris MCK Onlay Insert Extractor.

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Food

Reported Jun 13, 2018

Trader Joe's Artisan Bread - Organic French Baguette; (Brown and Serve) Keep frozen; Product code 53835; 24 x 11.5 oz.…

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

Trader Joes Company

FDA (openFDA food enforcement)

Medical devices

Reported Jun 6, 2018

Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators, Catalog No C650-129A (00821925008700) The cord consists…

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

Gyrus Acmi, Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), Part Number 0998-00-0800-XX & 0998-UC-0800-XX (excluding…

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

Maquet Datascope Corp. - Cardiac Assist Division

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.