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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 Jan 22, 2020

LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an…

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

Physio-Control, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 15, 2020

Hannaford brand Macaroni and Cheese, NET WEIGHT 12 OZ (340g); KEEP REFRIGERATED; UPC: 0 4126821062 6; Heating…

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

R. Walters Limited dba Meninno Brothers Foods

FDA (openFDA food enforcement)

Food

Reported Jan 15, 2020

GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G), UPC 8 53152 00308 1 , 4 OZ (113 G) UPC 8 53152…

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

TFI Holding dba Grey Ghost Bakery

FDA (openFDA food enforcement)

Medical devices

Reported Jan 8, 2020

i-STAT cTnI cartridge

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

Abbott Point Of Care Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 8, 2020

Classic Lays potato chips 2 3/4 oz. UPC 28400 42054; Classic Lays potato chips 8 oz. UPC 28400 19914; Classic Lays…

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

Frito-Lay, Inc.

FDA (openFDA food enforcement)

Food

Reported Jan 1, 2020

Trader Joe's 8pcs Spicy California Roll, 8oz, SKU 00348966T

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

Fuji Food Products, Inc.

22 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 25, 2019

Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…

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

Allergan PLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

Healix Knotless ADV BR 4.75 Suture Anchor

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

DePuy Mitek, Inc., a Johnson & Johnson Co.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943

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

Medtronic Navigation, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 11, 2019

Sullivan Harbor Farm Smokehouse Refrigerated, Ready-to-Eat, Cold Smoked Salmon in vacuum packaging (4 oz., 8 oz., 1…

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

Mill Stream Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 11, 2019

Color Cuff Disposable Tourniquet Cuff, 18 inch X 3 inch, 1BLA (Single Bladder), 1PRT(Single Port) Quick Connect…

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

Stryker Instruments Div.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2019

Atellica CH 930 Analyzer

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2019

EZ Glide Aortic Cannula, 24 Fr. (8.0mm) x 37.6 cm (14.8") 3/8" (9.5 mm) vented connector , RX Only, Sterile EC, Made in…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Food

Reported Nov 27, 2019

Dry dates packaged under the following brands: Keshav Dry Yellow Dates, 7oz., UPC: 643864233124 and 14oz., UPC:…

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

Peekay International, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 20, 2019

Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340…

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

Cadence Science, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2019

Prismaflex Control Unit, software versions below 7.21

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

Baxter Healthcare Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 13, 2019

Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar in 3.5 oz. foil wrapper packaging.

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

Dollar General Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Nov 13, 2019

The LivaNova VNS Therapy System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy…

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2019

Autoject EI, REF AJ1310

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

Owen Mumford USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…

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

Stryker Neurovascular

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

Posey Connected Twice-As-Tough Cuffs

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

Tidi Products

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

IMRIS MR/X-ray head fixation device, Model HFD200

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

Deerfield Imaging, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…

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

GE Healthcare, LLC

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.