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.

2,040 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.

Medical devices

Reported Jul 19, 2017

ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI…

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

Oscor, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 19, 2017

Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and…

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

Pentax

FDA (openFDA device enforcement)

Food

Reported Jul 12, 2017

Taste of Inspirations; Greek Pasta Salad, Net Wt. 10 oz.; Distributed By: DZA Brands, LLC, Salisbury, NC…

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

ASK Foods Inc.

FDA (openFDA food enforcement)

Food

Reported Jul 12, 2017

Tempo Seafood Bake - Lemon Dill- packaged in 3.5 oz. (99g), small corrugated boxes containing one pouch of breadcrumb…

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

Concord Foods, LLC

FDA (openFDA food enforcement)

Food

Reported Jul 12, 2017

Thin Cut Regular Batter: BLUE ACRES BATTERED ONION RINGS, NET WT. 10 lb (4.54 kg) - 33049; ATLANTIC GOLD BATTERED ONION…

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

Oxford Frozen Foods Plant 1

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 5, 2017

Whole Foods Cranberry Couscous- packaged in Clear plastic clamshell for 6oz, 14oz and 18oz, and white plastic pail for…

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

Hans Kissle Company, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 28, 2017

Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using…

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

Vascular Solutions, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 21, 2017

Philips DigitalDiagnost 3.1.x X-Ray System

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

Philips Electronics North America Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 7, 2017

The Acumed Slide-Loc Anatomic Radial Head System is intended for use by surgeons with orthopedic training. The device…

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

Acumed LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 7, 2017

NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)

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

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 7, 2017

Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;INFX-8000F

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

Toshiba American Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 31, 2017

Ceftriaxone TX 32 US S30, Ref 412302 and Ceftriaxone TX 32 US F100, Ref 507058 ETEST is a quantitative technique for…

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported May 31, 2017

CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000.

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

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 31, 2017

CORFLO, PEG Adaptor Repair Kit with ENFit Connectors, Size: 12FR (4mm); Product Usage: CORFLO PEG Tubes are intended…

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

CORPAK MedSystems, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the folding and delivering of the LI61AO, LI61AOV, or…

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

Bausch & Lomb Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 24, 2017

ETEST ETP32 (Ertapenem) Ref. 531640, 531600, blister packaging ETEST is a quantitative technique for determining the…

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported May 17, 2017

Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching

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

Arthrex, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 10, 2017

Shandon Rapid Chrome Kwik-Diff Kit Part Number: 9990700 Shandon Rapid Chrome Kwik-Diff Reagent #3 Part Number 9990707…

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

Richard-Allan Scientific Company

FDA (openFDA device enforcement)

Medical devices

Reported May 10, 2017

Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a…

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

Roche Diabetes Care, Inc.

FDA (openFDA device enforcement)

Food

Reported May 3, 2017

Apple Cider with Potassium Sorbate, packed under the following labels: RUDY'S BLEND APPLE CIDER; 1 GAL. (3.78L), UPC: 8…

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

Bevovations, LLC dba New England Apple Products Company

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 26, 2017

AFC Edamame Soybeans in Pods, 8 oz , refrigerated, in cardboard container. UPC 0-23012-00261-9

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

Advanced Fresh Concepts Corp.

FDA (openFDA food enforcement)

Food

Reported Apr 26, 2017

Asher's Chocolate Co, Milk Chocolate (11481) Pretzel Cluster; Net Wt. 5 lb.; Asher's Chocolate Co, Milk Chocolate…

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

Ashers Chocolates/Lewistown, Inc.

86 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 26, 2017

Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Vanilla; Product # PBP201 - 10-1.2 oz. packets;…

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

Nutiva

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 26, 2017

Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.

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

Teleflex Medical

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.