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.
2,040 stored notices name New Hampshire, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach New Hampshire too — those are in the archive.
Reported Aug 29, 2018
GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended for head, whole body,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare Japan Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Vision Care, Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Liebel-Flarsheim Company LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Chocolate Gooey Brownie Ice Cream, packaged in pint-sized containers (473 mL), net wt 378 g; 1 gal. container, or 3…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Salt & Straw LLC
FDA (openFDA food enforcement)
Reported Aug 22, 2018
Rio System Irrigation Clip - Catalog # 111690 Product Usage: The RESTORIS Partial Knee Application (PKA) for use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Aug 22, 2018
Severino Home Made, Artisanal Small Batch Pasta, Raviolini Cheese, 9 units x 9 oz per case. Expiration March 2019.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Severino Pasta Manufacturing, Inc.
FDA (openFDA food enforcement)
Reported Aug 15, 2018
Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Export For PTZ Video Ext, IP PTZ HD ErgoJust Video…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Matiz Raw Apricot Bar Demi-luna 8.8 ounces bar, packaged in shrink wrap plastic, UPC 8 32924 00543 0. Product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Power Selles Imports dba Culinary Collective
FDA (openFDA food enforcement)
Reported Aug 15, 2018
Ocean Delight Individually Vacuum Packed AHI TUNA SAKU, 8-12 oz. NET WT. 10 LB (4.54 kg) and 12-16 oz. NET WT. 22LB…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stavis Seafoods, Inc.
FDA (openFDA food enforcement)
Reported Aug 15, 2018
utz Carolina Style Barbeque Potato Chips, Net Wt 2.875 OZ, UTZ Quality Foods, LLV, Hanover, PA 17301, UPC:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Utz Quality Food Inc.
FDA (openFDA food enforcement)
Reported Aug 15, 2018
Waterpik Sonic-Fusion Professional, Model: SF-02 Product Usage: The device is composed of a unit base and an oral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Water Pik, Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Diagnostic Use Catalog No. 720-540
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Diamedix Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2018
MAYFIELD INFINITY XR2 BASE UNIT, Part Number A2079 The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Zimmer Dermatone AN, Model No. 88710100
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2018
AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N utilizing raw material (RM0677) from the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ad-Tech Medical Instrument Corporation
FDA (openFDA device enforcement)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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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.