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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 May 6, 2020

Lead diagnostic electrocardiograph under the following device names: ELI 10, ELI 350, ELI 150c, ELI 250c, ELI 230, ELI…

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

Welch Allyn, Inc/mortara

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 6, 2020

Whole Foods Market Minestrone Soup PLU code printed on the product scale labels beginning with 248529 for soup sold in…

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

Whole Foods Market

FDA (openFDA food enforcement)

Medical devices

Reported Apr 29, 2020

ARCHITECT HAVAB G Reagent Kit. List Number 6L27 25.

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

Abbott GmbH & Co. KG

FDA (openFDA device enforcement)

Medical devices

Reported Apr 29, 2020

Comprehensive Humeral Tray Taper Extraction Pliers - Replacement Tips, Model Number 110028522 - Product Usage: Intended…

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

Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 29, 2020

Fentanyl Reagent Kit, Product N. CC444, Contains: FENT R1 Reagent and FENT R2 Reagent

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

Carolina Liquid Chemistries Corp.

FDA (openFDA device enforcement)

Food

Reported Apr 29, 2020

Lake Champlain CHOCOLATES, COIN DARK BULK ORG, NET WT 48 OZ (1.3 kg), APPROX 186 PIECES, INGREDIENTS: DARK CHOCOLATE…

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

Champlain Chocolate Company

FDA (openFDA food enforcement)

Medical devices

Reported Apr 22, 2020

Merlin PCS 3650 Software Upgrade Kit, REF 3330 St. Jude Medical The MerlinTM Patient Care System (MerlinTM PCS) Model…

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

Abbott

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2020

Canon Aquilion Lightning, Model TSX-036A

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

Canon Medical System, USA, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

LabPro Data Management System, UDI: 15099590676872 - Product Usage: The LabPro Data Management System is a Microsoft…

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

Beckman Coulter Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

BIOMET StageOne Hip Cement Spacer Mold with Insert, 48 MM, Silicone, Sterile, Item 431181.

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

Biomet, Inc.

32 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

Firefly Floorsitter, Firefly Splashy Bathseat, Firefly GoTo Seat - Product Usage: The Splashy Bath-Seat is a Portable…

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

James Leckey Design Ltd.

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2020

Lindt & Sprungli (USA), Inc.; Excellence 85% Cocoa Dark Chocolate; Net WT 3.5OZ (100g)

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

Lindt & Sprungli (USA), Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 15, 2020

ABL800 FLEX, model number/UDI 393-800/0570 In Vitro testing of samples of whole blood for the parameters pH, pO2, pCO2,…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2020

Whole Foods Vodka Sauce, 6-16 oz. containers.

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

Winter Gardens Quality Foods, Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 8, 2020

Sushi Ebi Cooked Butterfly Tail-On Whiteleg Shrimp; Tray +0.498 pounds; 20 individual trays per case Distributed by AFC…

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

Advanced Fresh Concepts Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2020

BD WAVELINQ 4F EndoAVF System, Arterial Catheter 50 cm, Venous Catheter 43 cm, Sterile EO, Rx only, Mfr. Bard…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2020

Avalon Elite Vascular Access Kit, Model No. 70106.3540, UDI 04037691831039

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

Maquet Cardiovascular US Sales, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2020

Philips V60 Ventilators with Power Management PCBA part number 1055906

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

Respironics California, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2020

Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Tiger Cannulated…

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

Trilliant Surgical, LLC

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

Karl Storz NEURO-FIBERSCOPE, Model # 11282BN1, Flexible Pediatric Neuroscope

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

Karl Storz Endoscopy

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2020

CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG 545, BG CV545, BG 575, BG CV575, and…

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

CME America, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 25, 2020

Outshine Fruit Bars Strawberry; 6 Fruit Ice Bars; 14.7 Fl. oz. (435 mL) UPC: 041548610047 Case UPC: 10041548610044

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

Dreyers Grand Ice Cream, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 18, 2020

Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage: used for general…

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

Cardinal Health 200, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 18, 2020

Stonewall Kitchen, Ghost Pepper Salsa, Net Weight 454g (16oz), Ingredients: Tomatoes, Jalapeno Peppers, Onion, Tomato…

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

Stonewall Kitchen, LLC

FDA (openFDA food 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.