The Recall Desk

State

New Hampshire product recalls

73,833 recalls have nationwide distribution and so reach New Hampshire. 4,483 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,483
Critical
603
Severe
1,049
Most recent
2026-11-04

Of the 4,483 recalls naming New Hampshire we have scored against our rubric, 603 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,049 (23%) are Severe.

These figures cover only the 4,483 recalls whose distribution notice names New Hampshire specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51851–51875 of 78316

  • ModerateFDA (Devices)·Z-1575-2016·2016-05-04

    Mindray Panorama Patient Monitoring Network Recalled for Date Reversion

    Mindray DS USA is recalling Panorama Patient Monitoring Network units that may revert to the year 2000 during Daylight Savings Time.

    Product
    Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient Monitoring can view recal time, store, print, graph and trend patient clinical and demographic data. The Panoram Patient Monitoring Network can sent independent alarm limits for data send by the bedside…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1570-2016·2016-05-04

    BD Trucount Absolute Counting Tubes Recalled for Lot Mixing

    Becton, Dickinson and Company is recalling one lot of BD Trucount tubes because some pouches may contain tubes from a different lot, presenting a low risk to patient safety.

    Product
    BD Trucount Absolute Counting Tubes: Model number: 340334 IVD; BD Trucount tubes are used for determining absolute counts of leucocytes in blood. BD Trucount tubes are designed for use with in vitro diagnostic products such as BD Tritest reagents, and a suitably equipped…
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-1564-2016·2016-05-04

    Hansen Medical Recalls Magellan Robotic Catheter Accessory Kits

    Hansen Medical is recalling eight Magellan Robotic Catheter Accessory Kits because one batch was radiated below the required dose.

    Product
    Magellan Robotic Catheter Accessory Kits, Model number MACC 50 and MACC80. Cardiology: The Hansen Medical Magellan System is a robotic control system that enables positioning and visualization of a Magellan Catheter and an off-the-shelf guide wire while allowing a physician…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1261-2016·2016-05-04

    Family Gourmet Brown Rice Recalled Due to Live Insects

    Family Dollar is recalling Family Gourmet Natural Whole Grain Brown Rice because live insects were found in unopened bags.

    Product
    Family Gourmet Natural Whole Grain Brown Rice, 32 oz. (2 lb.) plastic bag (SKU: 1230394)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1527-2016·2016-05-04

    Corin Trinity Acetabular Shell Recalled for Packaging Abrasion Risk

    Corin USA Limited is recalling 629 Trinity Acetabular Shell devices used in total hip replacements due to a potential for abrasion of the sterile barrier pouches in the new packaging system.

    Product
    Trinity Acetabular Shell Product Usage: Total Hip Replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1246-2016·2016-05-04

    Bissinger's Milk Chocolate Eggs Recalled for Mislabeling Artificial Vanillin as Vanilla

    Karl Bissinger, LLC is recalling Bissinger's Milk Chocolate Eggs because the product contains artificial vanillin but is labeled as containing vanilla.

    Product
    Bissinger's Milk Chocolate Eggs packaged in 6.5 oz (UPC 846107009382) Item: #11108 or 1 lb. (UPC 846107003458) Item: # 111049 plastic bags. Bissinger's Handcrafted Chocolatier, St. Louis, MO.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1526-2016·2016-05-04

    Corin Trinity Acetabular System Recalled for Packaging Abrasion Risk

    Corin USA Limited is recalling 629 Trinity Acetabular System devices due to potential abrasion of sterile barrier pouches in the new packaging system.

    Product
    Trinity Acetabular System Product Usage - Total Hip Replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1566-2016·2016-05-04

    Stryker PneumoSure Insufflators Recalled for Flow Rate Drop

    Stryker Endoscopy is recalling PneumoSure insufflators because the flow rate drops to zero when connected to a house gas source, suspending insufflation.

    Product
    PneumoSure XL High Flow Insufflator and PneumoSure High Flow Insufflator; High pressure units (HPU) (40L and 45L). Model Numbers: 620-040-610, 620-040-611, 620-040-613, 620-040-614, 620-040-600, 620-040-601, 620-040-602, 620-040-604, 105-210-684 The Pneumo Sure XL High…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1266-2016·2016-05-04

    Bliss Bros Dairy Recalls Cresent Ridge Ice Cream for Air Space Issues

    Bliss Bros Dairy is recalling Cresent Ridge ChocChp CookiDgh WRAP Ice Cream because the product failed to meet air space specifications.

    Product
    Cresent Ridge ChocChp CookiDgh WRAP Ice Cream 48oz Product Code: 35403
    Category
    Food
    Distribution
    7 states
  • LowFDA (Food)·F-1282-2016·2016-05-04

    Bliss Bros Dairy Recalls Newport Creamery Butter Crunch Ice Cream

    Bliss Bros Dairy, Inc. is recalling Newport Creamery Butter Crunch Ice Cream because the product failed to meet air space specifications.

    Product
    Newport Creamery Butter Crunch Ice Cream, 3Gal Product Code: 35108
    Category
    Food
    Distribution
    7 states
  • LowFDA (Food)·F-1273-2016·2016-05-04

    Bliss Bros Dairy Recalls Emack & Bolios Ice Cream for Air Space Defect

    Bliss Bros Dairy is recalling Emack & Bolios Serious Choc Addiction Ice Cream because the product failed to meet air space specifications.

    Product
    Emack & Bolios Serious Choc Addiction Ice Cream 3gal Product Code: 36271
    Category
    Food
    Distribution
    7 states
  • LowFDA (Food)·F-1275-2016·2016-05-04

    Emack & Bolios Ice Cream Recalled for Air Space Specification Failures

    Bliss Bros Dairy is recalling Emack & Bolios Caramel Moose Prints Ice Cream because the product failed to meet air space specifications.

    Product
    Emack & Bolios Caramel Moose Prints Ice Cream, 3gal Product Code: 36285
    Category
    Food
    Distribution
    7 states
  • LowFDA (Food)·F-1279-2016·2016-05-04

    Bliss Bros Dairy Recalls Pistachio Ice Cream for Packaging Defect

    Bliss Bros Dairy is recalling Emack & Bolios Pistachio Ice Cream because the product failed to meet air space specifications.

    Product
    Emack & Bolios Pistachio Ice Cream, 3gal Product Code: 36262
    Category
    Food
    Distribution
    7 states
  • LowFDA (Food)·F-1269-2016·2016-05-04

    Bliss Bros Dairy Recalls Cresent Ridge Choc Chip Cookie Dough

    Bliss Bros Dairy is recalling 5 units of Cresent Ridge Choc Chip Cookie Dough because the product failed to meet air space specifications.

    Product
    Cresent Ridge Choc Chip Cookie Dough 48oz Product Code: 35418
    Category
    Food
    Distribution
    7 states
  • LowFDA (Devices)·Z-1582-2016·2016-05-04

    Teleflex Pleur-evac Chest Drainage System Recalled for Missing Tyvek Bag Label

    Teleflex Medical is recalling Pleur-evac Chest Drainage Systems because the Tyvek bag label is missing, preventing identification of material code, lot number, and expiration date.

    Product
    Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only, Teleflex Medical. Product Usage: Pleur-Evacs are sterile, single-use, chest drainage systems intended for post-operative use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0834-2016·2016-05-04

    SKY Aspirin Chewable Tablets Recalled for Incorrect Outer Carton Labeling

    McKesson Packaging Services is recalling SKY Aspirin Chewable Tablets because the outer cartons were incorrectly labeled. The recall addresses a labeling mix-up.

    Product
    SKY Aspirin Chewable Tablets, 81 mg, Unit Dose 750 tablets (25 x 30) box, OTC, Distributed by: McKesson Packaging Service, Concord, NC 28027, NDC 63739-434-01.
    Category
    Drug
    Distribution
    Distributed nationwide