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.

2,036 stored notices name New Hampshire, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach New Hampshire too — those are in the archive.

Medical devices

Reported Feb 19, 2020

Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been serviced with the following: Pacific…

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

Pacific Medical Group Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2020

Bulk Pail Product -- Almark Foods HARD COOKED BROKEN EGG WHITES 20 LB pail, DIST BY: ALMARK FOODS, GAINESVILLE, GA…

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

Almark Foods, LLC

28 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 12, 2020

Ducktrap River of Maine Herring Center Cuts in Wine Sauce, 12 oz.

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

Ducktrap River

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2020

Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob, 2264HAX, FFCM3205

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

Pacific Medical Group Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

CS5/5+ Fastpacks, 225 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are…

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

Haemonetics Corporation

21 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2020

Jeni's Dairy Free Cold Brew with Coconut Cream Pints frozen dessert

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

Jeni's Splendid Ice Creams LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2020

Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14

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

Johnson & Johnson Surgical Vision Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2020

AQURE basic sytem, FLEXLINK, REF 933-599, Version: 2.3.3 (17), CE IVD, Rx Only, UDI: (01)05700699335999 Intended use:…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Food

Reported Jan 22, 2020

13 Bean Soup Mix is sold under Bob's Red Mill brand, packaged in Form & Fill (29 oz. and 822 gram), Standup Pouch (29…

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

Bob's Red Mill Natural Foods, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 22, 2020

ADVANCED ENDOSEE System CANNULA, Cooper Surgical Product Code/Model Number: ESPX5 The Advanced Endosee Cannula…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2020

QuickDraw Venous Cannula, REF: QD22, UDI: 00690103182699; and REF: QD25, UDI: 00690103182705

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

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)

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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.