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.

Which agencies issued them

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.

50376–50400 of 78316

  • ModerateFDA (Devices)·Z-2225-2016·2016-07-27

    WalkMed Recalls IV Administration Sets Due to Potential Particulate Presence

    WalkMed Infusion is voluntarily recalling specific IV administration sets due to the potential presence of particulate matter in or on the devices.

    Product
    T090-000W 90" 20 Drop IV Admin Set w/2 Needlefree Y-Sites Back Check Valve. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2241-2016·2016-07-27

    CSL Behring Recalls Dimension Vista Homocysteine Reagent Cartridges

    CSL Behring is recalling 898 units of Dimension Vista Homocysteine Flex Reagent Cartridges because opened lots show reduced stability and do not meet the 7-day claim.

    Product
    Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS), Device Listing No.: D017878 is an in vitro diagnostic test for the quantitative measurement of total homocysteine in human serum, heparinized plasma and EDTA plasma on the Dimension Vista System.
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-2239-2016·2016-07-27

    Hologic Recalls ATEC Suction Canisters Due to Cracked Lids

    Hologic is recalling 16,870 ATEC Suction Canisters because the lids may crack. These devices are used to collect fluid during breast biopsies.

    Product
    ATEC CANISTER. Suction Canister with Lid 490 cc., RX Only; Suction canister used to collect fluid during a breast biopsy.
    Category
    Medical Device
    Distribution
    52 states
  • ModerateFDA (Devices)·Z-2220-2016·2016-07-27

    WalkMed Infusion Pumps Recalled for Unapproved Software and Specification Changes

    WalkMed Infusion is recalling Triton and Triton FP infusion pumps due to unapproved changes to software, specifications, and intended use.

    Product
    The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper for distribution.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1705-2016·2016-07-27

    Bolthouse Farms Recalls Protein Plus Drinks Due to Spoilage

    Bolthouse Farms is recalling eight varieties of Protein Plus and Perfectly Protein drinks because spoilage may cause the beverages to appear lumpy and have an unpleasant taste and odor.

    Product
    Bolthouse Farms Strawberry Protein Plus: 30 g protein per bottle + 21 vitamins & minerals. Packaged in 15.2 oz/450 mL item number: PPCN4BF6; 32 oz/946 mL. - item number PPSWQBF6 Selling Unit UPC Case GTIN 15.2 oz.…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2214-2016·2016-07-27

    DePuy Synthes Recalls TFNA Blade/Screw Guide Sleeves Due to Sizing Defect

    DePuy Synthes is voluntarily recalling TFNA Blade/Screw Guide Sleeves because a manufacturing defect may prevent proper use, potentially causing surgical delays.

    Product
    Depuy Synthes Trauma- Trochanteric Fixation Nail Advanced (TFNA) Blade/Screw Guide Sleeve, Surgical Instrument Part Number ID 03.037.017, Class I exempt Lot Numbers: 9066399; 9066435; 9409790; 9519308; 9620447; 9301183; 9409792; 9519303; 9641077; 9301184; 9409791; 9542998…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2208-2016·2016-07-27

    Terumo Recalls Sarns Temperature Control Units Due to Sanitizer Discontinuation

    Terumo CVS is voluntarily recalling Sarns TCM units because the Interchlor sanitizer referenced in cleaning instructions is no longer sold by the distributor.

    Product
    Sarns TCM; The Sarns Temperature Control and Monitor unit (TCM) is a source of temperature-controlled water for blood heat exchangers used in an extracorporeal circuit and for blankets to externally heat or cool the patient The TCM with options will also supply water for…
    Category
    Medical Device
    Distribution
    51 states
  • LowFDA (Drugs)·D-1446-2016·2016-07-27

    Sun Pharmaceutical Recalls Bupropion Hydrochloride Tablets for Dissolution Failure

    Sun Pharmaceutical Industries is recalling 16,085 bottles of Bupropion Hydrochloride Extended Release Tablets because they failed dissolution specifications.

    Product
    BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V558000·2016-07-26

    Forest River Recalls 2011-2016 Glaval Titan II Buses for Frame Cracks

    Forest River is recalling 39 Glaval Titan II Low Floor buses due to frames that may crack, potentially reducing driver control and increasing crash risk.

    Product
    GLAVAL BUS — GLAVAL BUS TITAN II LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V559000·2016-07-26

    2015 RAM 2500 and 3500 Recalled for Steering Bracket Weld Defect

    Chrysler is recalling 2015 RAM 2500 and 3500 trucks because inadequate welds on front track bar brackets may separate, reducing steering response and increasing crash risk.

    Product
    RAM — RAM 2500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V557000·2016-07-26

    Load Trail Triple Axle Tilt Deck Trailers Recalled for Weld Defects

    Load Trail is recalling 2014-2016 Triple Axle Tilt Deck trailers because weld joints may crack, potentially causing equipment to disengage and increasing crash risk.

    Product
    LOAD TRAIL — LOAD TRAIL TRIPLE AXLE TILT DECK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·065-2016·2016-07-26

    PT Farm Recalls Raw Beef Products Due To Possible E. Coli O157:H7 Contamination

    PT Farm, LLC is recalling approximately 8,800 pounds of raw beef products due to possible E. coli O157:H7 contamination linked to an illness cluster.

    Product
    Montshire Packing, LLC — PT Farm, LLC Recalls Beef Products Due To Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    4 states
  • HighCPSC·16759·2016-07-26

    Electrolux Recalls Frigidaire and Kenmore Wall Ovens Due to Fire Hazard

    Electrolux is recalling about 1,000 Frigidaire and Kenmore electric wall ovens because a malfunctioning thermal switch poses a fire hazard. No injuries have been reported.

    Product
    Electric wall ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16760·2016-07-26

    Inovonics Recalls Emergency Transmitters and Receivers Due to Signal Failure

    Inovonics is recalling about 5,500 emergency transmitters and receivers because they may fail to send or receive help signals. No injuries have been reported.

    Product
    Inovonics pendant transmitters, universal transmitters and add-on receivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E065000·2016-07-25

    ZF Transmission Sensor Clusters Recalled for Unexpected Neutral Shifts

    ZF North America is recalling certain 9-speed automatic transmission sensor clusters due to insufficient wire harness crimps that may cause the vehicle to unexpectedly shift to neutral.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION:CONTROL MODULE (TCM/PCM/TECM) recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V553000·2016-07-25

    BMW Recalls 2016-2017 MINI Clubman for Side Air Bag Defect

    BMW is recalling 2016-2017 MINI Clubman vehicles because side curtain air bags may not deploy correctly in a crash, increasing injury risk.

    Product
    MINI — MINI CLUBMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V550000·2016-07-22

    2017 Coachmen Freedom Express Recalled for Tire Rubbing Hazard

    Forest River is recalling 2017 Coachmen Freedom Express recreational vehicles because insufficient space between the driveshaft and tires may cause tire failure and loss of control.

    Product
    COACHMEN — COACHMEN FREEDOM EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V548000·2016-07-22

    Mitsubishi Outlander Sport Recall for CVT Hose Clamp Defect

    Mitsubishi is recalling 2015 Outlander Sport vehicles because a CVT hose clamp may not be secured, risking fluid leaks, inoperability, or fire.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide