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.

2,034 stored notices name New Hampshire, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach New Hampshire too — those are in the archive.

Medical devices

Reported Jul 8, 2026

Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips…

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

Teleflex LLC

FDA (openFDA device enforcement)

Drugs

Reported Jul 8, 2026Updated Sep 16, 2026

Apheresis Platelets, Leukocytes Reduced

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

The Blood Connection, Inc.

FDA (weekly enforcement report)

Medical devices

Reported Jul 1, 2026

Da Vinci ASSY, PSS, SP1098, Part Number: 380601

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2026

Dried Herring Fish 7 oz.

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

Prime Food Processing LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2026

INZONE DETACHMENT SYSTEM, REF: M00345100950

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU

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

Arrow International, LLC

34 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

iLet Bionic Pancreas, REF: BB1001

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

Beta Bionics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 00884450529669 00884450529690 REF:…

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

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

Mito Red Light, Super Mobile

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

Mito Red Light Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product Description: The STAAR ICL…

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

Staar Surgical AG

FDA (openFDA device enforcement)

Medical devices

Reported Jun 17, 2026

Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software

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

Abbott Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jun 17, 2026

Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52…

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

HF Acquisition Co. LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 17, 2026

Individual Unit Label (both lid and front of cup): Whole Foods Market Kitchens Minestrone Soup, VEGETARIAN NET WT 24 OZ…

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

Kettle Cuisine, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 10, 2026

Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description:…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 10, 2026

BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose…

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

Becton Dickinson & Company

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 10, 2026

Birch Benders Sweet Potato Pancake and Waffle Mix 12oz bag, UPC 8 1000156076 8, 6 bags per case

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

Hometown Food Company

FDA (openFDA food enforcement)

Medical devices

Reported Jun 10, 2026

Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 10, 2026

Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor…

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

Kico Knee Innovation Company

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 10, 2026

1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0399549125016 2) Cheese…

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

The Coffee Connexion Co., Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 27, 2026

Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7,…

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

Becton, Dickinson and Company

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 27, 2026

Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley…

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

C.R. Bard Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 27, 2026

Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros;…

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

ICU Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported May 27, 2026

Pork King Good Onion & Sour Cream Seasoning. Net Wt. 3 oz (85G) bottle. UPC 8 50008-53861 2. Made by Pork King Good,…

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

Pork King Good, LLC

FDA (openFDA food enforcement)

Medical devices

Reported May 20, 2026

Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number:…

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

Dexcom, Inc.

2 more products in this recall

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.