The Recall Desk

State

New Hampshire product recalls

73,106 recalls have nationwide distribution and so reach New Hampshire. 4,472 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,472
Critical
606
Severe
858
Most recent
2026-09-23

Of the 4,472 recalls naming New Hampshire we have scored against our rubric, 606 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 858 (19%) are Severe.

These figures cover only the 4,472 recalls whose distribution notice names New Hampshire specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12451–12475 of 77578

  • HighFDA (Devices)·Z-1279-2024·2024-03-20

    D-Clip Surgical Applier Recalled for Failure to Release During Surgery

    FDA has recalled the D-Clip Standard/Mini Applier due to reports that the device failed to release the clip and remained attached during surgical use, creating a risk of surgical complications.

    Product
    D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0384-2024·2024-03-20

    FDA Recalls HylaTears Lubricant Eye Drops for Sterility Assurance Issue

    Optikem International is recalling 46,621 bottles of hyalogic For Dry Eyes, HylaTears Lubricant Eye Drops due to lack of assurance of sterility. The product is distributed nationwide.

    Product
    hyalogic For Dry Eyes, HylaTears", Lubricant Eye Drops, 0.67 FL OZ (20mL) bottle, Manufactured for hyalogic, 610 NW Platte Valley Dr., Riverside, MO 64150
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0377-2024·2024-03-20

    Eye Drops Recall: TRP Eye Twitching Relief Lacks Sterility Assurance

    TRP Eye Twitching Relief sterile eye drops are being recalled nationwide because the manufacturer cannot assure the product meets sterility requirements. The affected lot (C303, expiring 07-27-2025) was distributed in the USA.

    Product
    TRP Eye Twitching Relief, Sterile Eye Drops, Homeopathic 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-040-15.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1282-2024·2024-03-20

    Infusion Pump Software Defect Causes Incorrect Alarm and Therapy Delay

    Fresenius Kabi is recalling software versions 5.0.1 and earlier of the Ivenix Infusion System due to a software defect that may cause an incorrect pump alarm, potentially delaying therapy. The defect was resolved in software version 5.2.1, released in September 2022.

    Product
    LVP software of the Ivenix Infusion System (IIS), LVP-SW-0004
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1294-2024·2024-03-20

    BVI Visitec Irrigation Handle lacks manufacturing and expiration dates

    Beaver Visitec International is recalling 3,000 BVI Visitec Irrigation Handles because the pack and pouch labels are missing manufacturing and expiration date information.

    Product
    BVI Visitec Irrigation Handle (20/SP)- Intended to be fit with a cannula for irrigation of the eye Catalog Number: 581012
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1298-2024·2024-03-20

    Hip prosthesis labeling clarification needed to prevent surgical confusion

    Waldemar Link is clarifying labeling on 153 hip prosthesis units after complaints about ambiguous Size and Type information. The guidance aims to prevent potential misinterpretation during surgery.

    Product
    SPII Model Lubinus, Long Stem Prosthesis Standard Neck, cemented
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0386-2024·2024-03-20

    Broncochem Cold & Flu Syrup Kids Recalled Due to Stability Testing Failures

    Global Corporation is recalling Broncochem Cold & Flu Syrup Kids (120 mL bottles) nationwide due to stability testing failures in active pharmaceutical ingredients.

    Product
    Broncochem Cold & Flu Syrup Kids (acetaminophen, guaifenesin, phenylephrine HCl), packaged in 120 mL bottles, Made in Dominican Republic Exclusively for Global Corporation Inc, Boca Raton, FL 33187 USA, NDC 65131-098-44
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0387-2024·2024-03-20

    FDA Recalls Broncochem Cold & Tea Nationwide for Stability Failures

    Global Corporation is recalling Broncochem Cold & Tea nationwide due to stability testing failures in the active ingredients. No illnesses or injuries have been reported.

    Product
    BRONCOCHEM — BRONCOCHEM (ACETAMINOPHEN-PHENYLEPHRINE HYDROCHLORIDE-CHLORPHENIRAMINE MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1287-2024·2024-03-20

    Aneurysm clips recalled due to incorrect blue coloring

    Peter Lazic Gmbh is recalling 170 L-Aneurysm Clip TITANIUM Paddle-Clips distributed in Maine due to incorrect blue coloring instead of blank.

    Product
    L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0369-2024·2024-03-20

    Febuxostat tablets recalled due to microbial contamination in manufacturing

    Sun Pharmaceutical is recalling 7,488 bottles of Febuxostat 80mg tablets nationwide due to microbial contamination found in manufacturing equipment. No illnesses have been reported.

    Product
    FEBUXOSTAT — FEBUXOSTAT (FEBUXOSTAT)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1288-2024·2024-03-20

    Aneurysm clips recalled due to incorrect paddle coloring

    Peter Lazic Gmbh is recalling 51 titanium aneurysm clip paddle clips because the clips are colored blue when they should be blank.

    Product
    L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V209000·2024-03-19

    2024 Alfa Romeo Tonale vehicles with missing tire and rim label information

    Chrysler is recalling certain 2024 Alfa Romeo Tonale vehicles because the manufacturer label is missing tire rim and tire size information, which could lead to incorrect wheel installation and increase crash risk.

    Product
    DODGE — DODGE, ALFA ROMEO HORNET, TONALE PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V210000·2024-03-19

    Cruiser Avenir Trailers Recalled for Missing Tire Certification Labels

    Cruiser RV is recalling 2023-2024 Avenir trailers because Federal Certification labels lack tire size and PSI data, potentially leading to incorrect tire installation or inflation.

    Product
    CRUISER — CRUISER AVENIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V212000·2024-03-19

    2023–2024 Jayco and Entegra Motorhomes Rearview Camera Failure Recall

    Jayco, Inc. is recalling certain 2023–2024 Jayco Solstice and Entegra Expanse motorhomes built on Ford chassis because the rearview camera may not display an image when in reverse, reducing rear visibility and increasing crash risk.

    Product
    JAYCO — JAYCO, ENTEGRA SOLSTICE LI, SOLSTICE, EXPANSE LI, EXPANSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V203000·2024-03-17

    2021–2023 Nova Bus LFS Buses Power Cable Nut Fire Risk

    Nova Bus is recalling certain 2021–2023 LFS buses because the alternator power cable nut may not have been tightened properly, increasing the risk of electrical arcing and fire.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V207000·2024-03-15

    Mercedes-Benz Recalls Vehicles Due to 48-Volt Ground Connection Fire Risk

    Mercedes-Benz is recalling specific 2019-2024 models because a 48-Volt ground connection may overheat, increasing the risk of a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH AMG GLE53, AMG GLE63 S 4MATIC+, GLS 600, GLS 600 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V205000·2024-03-15

    2024 Genesis GV70 Transmission Recall Due to Water Intrusion Risk

    Certain 2024 Genesis GV70 vehicles are recalled because water may leak into the transmission control harness, causing electrical shorts that shift the transmission from Park to Neutral, risking vehicle rollaway.

    Product
    GENESIS — GENESIS GV70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V202000·2024-03-15

    Dynamax Isata Motorhomes Recalled for Loose 12V Disconnect Fire Risk

    Dynamax Isata motorhomes (2023-2024) are recalled for a loose 12V disconnect nut that may cause electrical arcing and fire risk. Dealers will replace the part free of charge.

    Product
    DYNAMAX — DYNAMAX ISATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V204000·2024-03-15

    Hyundai and Genesis electric vehicles recalled for 12-volt battery charging failure

    Hyundai is recalling certain 2023 Ioniq 6 and related Genesis models because the 12-volt battery charger may fail, causing potential loss of drive power and increased crash risk. Repairs will be completed free of charge.

    Product
    HYUNDAI — HYUNDAI, GENESIS IONIQ 6, IONIQ 5, GV70 ELECTRIFIED, GV60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V198000·2024-03-14

    Chrysler 300 and Dodge Charger side curtain airbag defect recall

    Certain 2018-2021 Chrysler 300 and Dodge Charger vehicles are being recalled for defective side curtain airbag inflators that may rupture. Dealers will replace both airbags free of charge.

    Product
    CHRYSLER — CHRYSLER, DODGE 300, CHARGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E025000·2024-03-14

    Chrysler Recalls Steering Column Modules for Air Bag Deployment Risk

    Chrysler is recalling MOPAR steering column control modules used in 2017-2024 Jeep, Chrysler, and Ram vehicles because improper welding may prevent the driver's air bag from deploying.

    Product
    AIR BAGS:FRONTAL:DRIVER CLOCKSPRING/SPIRAL CASSETTE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V199000·2024-03-14

    2023-2024 Jeep Wrangler and Ram Vehicles Steering Module Airbag Defect

    Chrysler is recalling 2023-2024 Jeep Wrangler, Ram, Pacifica, and other vehicles because a faulty steering column control module may prevent driver airbag deployment in a crash. Dealers will replace the module free of charge.

    Product
    RAM — RAM, JEEP, CHRYSLER 1500, 2500, 5500, WAGONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E024000·2024-03-14

    Chrysler Recalls Side Curtain Air Bag Inflators Due to Rupture Risk

    Chrysler is recalling specific MOPAR side curtain air bag inflators sold as replacement parts for 2011-2020 vehicles due to a manufacturing defect that may cause rupture.

    Product
    AIR BAGS:SIDE/WINDOW:CURTAIN:INFLATOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide