The Recall Desk

State

New Hampshire product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43051–43075 of 78300

  • SevereCPSC·18037·2017-11-16

    Arctic Cat Recalls Wildcat ROVs Due to Winch Fire Hazard

    Arctic Cat is recalling 2017 Wildcat ROVs and winch kits because the winch solenoid can overheat and cause fires. No injuries have been reported.

    Product
    Arctic Cat ROVs with winches
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V722000·2017-11-16

    Spartan Recalls 2014-2017 Emergency Vehicles Due to Pressure Valve Defect

    Spartan Motors is recalling 2014-2017 Gladiator and MetroStar emergency vehicles because corroded rings may cause pressure relief valves to open, reducing water pressure for firefighting.

    Product
    SPARTAN — SPARTAN METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0132-2018·2017-11-15

    Stonyfield Organic Soy Yogurt Recalled for Undeclared Milk

    Stonyfield Farm is recalling 17,688 cups of Organic O'soy Strawberry on the Bottom Soy Yogurt because the product may contain undeclared milk.

    Product
    Stonyfield ORGANIC O'soy Strawberry on the bottom SOY YOGURT 5.3 Oz (150g), UPC Codes: 0-52159-00603-7. KEEP REFRIGERATED
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-0083-2018·2017-11-15

    Teleflex Auto Endo5 Clip Applier Recalled for Clip Misalignment

    Teleflex Medical is recalling 13,710 units of the Auto Endo5 Automatic Hem-o-lok Clip Applier because clips may misalign, jam, or fall out of the device.

    Product
    WECK(R) from TELEFLEX Auto Endo5(R), Automatic Hem-o-lok(R) Clip Applier, REF AE05ML (IPN010797) Rx ONLY, STERILE EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0347-2018·2017-11-15

    21st Century Snack Foods Recalls Dark Chocolate Almonds for Undeclared Milk

    21st Century Snack Foods is recalling Dark Chocolate Almonds because the product contains undeclared milk, a major food allergen.

    Product
    21st CENTURY SNACK FOODS DARK CHOCOLATE ALMONDS Roasted Almonds Covered in Rich Dark Chocolate Net Wt. 6oz (170g) UPC: 0 30603 22854 9.
    Category
    Food
    Distribution
    49 states
  • HighFDA (Devices)·Z-0075-2018·2017-11-15

    Terumo BCT Recalls Harvest Graft Delivery Packs Due to Seal Defect

    Terumo BCT is recalling 525 Harvest Graft Delivery Packs because some lots may lack a seal on the inner pouch, potentially compromising sterility.

    Product
    HARVEST TERUMOBCT, GCP-10 Graft Delivery Pack, REF 51449, Rx Only, STERILE EO Harvest Graph Delivery System is a disposable pack that takes the cell concentrate created while using the BMAC Procedure Packs and allows for hydration of bone graft material for application to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0076-2018·2017-11-15

    Sorin FlexFlow Venous Cannula Recalled for Sharpness Defect

    Sorin Group USA is recalling a specific lot of FlexFlow Venous Cannulas because they are sharper or pointier than expected.

    Product
    FlexFlow Venous Cannula Model/Catalog Number 200-200 The FlexFlow Venous Cannula is a single use sterile device. It is a size 23 French with an outside diameter of 0.30 inch (7.7 mm) and an effective working length of 11.2 inch (28.5 cm). The FlexFlow Venous Cannula is an open…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0065-2018·2017-11-15

    Encore Medical Recalls Cobalt MV Bone Cement Due to Packaging Seal Loss

    Encore Medical is recalling 840 units of Cobalt MV Bone Cement because the sterile Tyvek packaging seal may be lost, potentially compromising sterility.

    Product
    Cobalt MV Bone Cement 40GM, REF 402438, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0067-2018·2017-11-15

    Encore Medical Recalls Cobalt Bone Cement Due to Packaging Seal Loss

    Encore Medical, Lp is recalling Cobalt HV with Gentamicin bone cement because the sterile Tyvek packaging may have lost its seal, potentially compromising sterility.

    Product
    Cobalt HV with Gentamicin, Cobalt Bone Cement 40GM, REF 402283, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0084-2018·2017-11-15

    BD Vacutainer Blood Collection Tubes Recalled for Incorrect Labeling

    Becton Dickinson is recalling 90,000 blood collection tubes due to incorrect labeling at the case and shelf pack level.

    Product
    BD Vacutainer Sodium Polyanetholesulfonate 5.95 mg Sodium Chloride 14.4 mg Blood Collection Tubes for Microbiological Studies (8.3 mL * 16x100mm) Catalog No. 364960
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0066-2018·2017-11-15

    Encore Medical Recalls Cobalt Bone Cement Due to Packaging Seal Loss

    Encore Medical, Lp is recalling 1,815 units of Cobalt MV with Gentamicin bone cement because the sterile Tyvek packaging seal was lost.

    Product
    Cobalt MV with Gentamicin, Cobalt Bone Cement 40GM, REF 402439, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0064-2018·2017-11-15

    Biomet Cobalt HV Bone Cement Recalled for Packaging Seal Loss

    Encore Medical is recalling Biomet Cobalt HV Bone Cement because the sterile Tyvek packaging seal may be lost, potentially compromising sterility.

    Product
    Cobalt HV Bone Cement 40GM, REF 402282, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0071-2018·2017-11-15

    Aaren Scientific AERO IOL Injection System Recalled for Incorrect Storage Labeling

    Aaren Scientific Inc. is recalling 786 boxes of AERO IOL Injection Systems because the recommended storage temperature on the label is incorrect.

    Product
    AERO IOL Injection System containing 10 Z28 Cartridges per box, Part #003500-0025-282, Sterile, Rx. The firm name on the label is Aaren Scientific Inc., Ontario, CA. Used to fold and insert the firm's IOL's.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0072-2018·2017-11-15

    Doan's Pain Relieving Cream Recalled for Packaging Labeling Mismatch

    Dr. Reddy's is recalling Doan's Pain Relieving Cream because the lot number on the outer packaging does not match the bottle. This is a Class III labeling recall.

    Product
    Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol, (lidocaine 4%, menthol 1%), Net Wt. 2.75 oz. (77.3 g) Tube, Distributed by: Ducere Pharma, LLC New Hope, PA 18938 USA --- UPC 849648000023
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V714000·2017-11-14

    Mercedes-Benz Recalls 2017 Models for Power Steering Overheating Risk

    Mercedes-Benz is recalling 72 vehicles from 2017 models due to a power steering control unit defect that may disable assist, increasing crash risk.

    Product
    MERCEDES-MAYBACH — MERCEDES-MAYBACH, MERCEDES-BENZ S600, S65 AMG, E300, S550
    Category
    Vehicle
    Distribution
    Distributed nationwide