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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 14, 2021

Synapse PACS - Radiological Image Processing System - Product Usage: intended for use, as a web based application, on…

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

Fujifilm Medical Systems U.S.A., Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 14, 2021

Panther Fusion Tube Tray, REF PRD-04000, PN: FA-15004, Cont. 18 Tube Trays - Product Usage: an ancillary consumable to…

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

Hologic, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 14, 2021

Consist of a distal connection mechanism (either standard Terumo Ball Quick Connect or Terumo Shaft Quick Connect), an…

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

Terumo Cardiovascular Systems Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 7, 2021

ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually packaged femoral, tibial and patellar components…

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

DePuy Orthopaedics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 7, 2021

Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 31, 2021

BARD MARQUEE Disposable Core Biopsy Instruments XX.Xcm, XX.Xcm, XXg x XXcm REF XXXXXXX Note - for definition of the…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 31, 2021

In-View Clear Leggings Sterile

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

Cardinal Health 200, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 31, 2021

Operating Table System

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

Getinge Group Logistics America, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 31, 2021

Duodenoscope and accessories, flexible/rigid - Product Usage: used with an Olympus video system center, light source,…

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Mar 31, 2021

S-Series Equipment Management System; Model Number(s):0682400550; UDI: 07613327400502 Components that are affected…

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

Stryker Communications

FDA (openFDA device enforcement)

Medical devices

Reported Mar 31, 2021

RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct visualization of the laryngeal structure and is…

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

Teleflex Medical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 17, 2021

Prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer.

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

Howmedica Osteonics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 17, 2021

PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2 defibrillator is designed for indoor and outdoor…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 17, 2021

Dimension Vista HDLC - colorimetric method, lipoproteins - Product Usage: used as an aid in the diagnosis of lipid…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 17, 2021

Old Cape Cod Soup and Chowder Oyster Crackers - 8oz Box, 12 per case - UPC 093215801005; Westminster Bakers Co. Soup &…

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

Westminster Cracker Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 10, 2021

The PrisMax System Version II Hemodialysis Delivery System: Automatic Repositioning System Pump Assembly, specifically…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

Band, Elastic, Orthodontic - Product Usage: Orthodontic elastics, also referred to as rubber bands, are small stretchy…

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

G & H Wire Company

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

HAMILTON HEATER SHAKER, 115 VAC/ 230 VAC, 750 VA, Power Consumption 41V/ 100W (max.), Relative Humidity 15% - 85% no…

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

Hamilton Co.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

WMTS Telemetry Receiver, Multiple Patient Receiver, Model Number/ UDI: ORG 9100A/ 00841983102554 ORG 9110A/…

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

Nihon Kohden America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

Infusion Pump

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

VITROS Chemistry Products VersaTips - Product Usage: used to dispense samples to MicroSlide assays and sample and…

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

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

ENROUTE Transcarotid Stent System REF SR-XXYY-CS

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

Silk Road Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 24, 2021

IOLMaster 700

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

Carl Zeiss Meditec AG

FDA (openFDA device enforcement)

Medical devices

Reported Feb 24, 2021

Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCC)V-402a - Product Usage: is a lateral…

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

Confirm Biosciences 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.