The Recall Desk

State

New Hampshire product recalls

73,738 recalls have nationwide distribution and so reach New Hampshire. 4,482 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,482
Critical
603
Severe
1,048
Most recent
2026-10-28

Of the 4,482 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 1,048 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,482 recalls whose distribution notice names New Hampshire specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33426–33450 of 78220

  • ModerateFDA (Devices)·Z-0053-2020·2019-10-16

    Arrow Pediatric Central Venous Catheter Kit Recalled for Labeling Error

    Arrow International Inc. is recalling 3,143 Pediatric Two-Lumen Central Venous Catheterization Kits due to a labeling error on the lidstock.

    Product
    Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, REF AK-25502 Product Usage; Provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0113-2020·2019-10-16

    GE Healthcare Recalls Achilles Express Bone Sonometers Due to Power Cord Issue

    GE Healthcare is recalling 241 Achilles Express Bone Sonometers because they were shipped with power cords that do not meet local safety requirements for protective earth connection.

    Product
    Achilles Express Bone Sonometer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0109-2020·2019-10-16

    Roche Tina-quant sTfR Assay Recalled for Rheumatoid Factor Interference

    Roche Diagnostics is recalling Tina-quant Soluble Transferrin Receptor (sTfR) assays due to updated claims regarding rheumatoid factor interference.

    Product
    cobas c 701 and 702 Analyzer/Module-RF interference claims for the sTfR assay Catalog Number: 05950821190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0132-2020·2019-10-16

    DrKids Children's Natural Cough Syrup Recalled for Potential B. cepacia Contamination

    Unipharma, LLC is recalling DrKids Children's Natural Cough Syrup due to a precautionary measure regarding potential contamination with B. cepacia bacteria.

    Product
    DrKids Children's Natural Cough Syrup English Ivy Leaf, packaged in Pre-measured Single-Use Vials 0.17 fl. oz. (5 mL) Each 3.4 fl. oz. (100 mL), Manufactured in USA by: UNIPHARMA, LLC Tamarac, FL 33321 UPC 370302489026
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0061-2020·2019-10-16

    BD Microtainer Tubes Recalled Due to Damaged Reservoirs

    Becton Dickinson is recalling specific lots of BD Microtainer Tubes with FE Glycolytic Inhibitor because damaged reservoirs may cause insufficient sample volumes and erroneous test results.

    Product
    BD Microtainer Tubes with FE (Sodium Fluoride / Disodium EDTA) Glycolytic Inhibitor Part/Catalog Number: 365992
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0137-2020·2019-10-16

    Guerbet Recalls Optiray Syringes Due to RFID Formatting Error

    Guerbet LLC is recalling 3,860 Optiray syringes because an RFID formatting error causes the injector to read the product as expired, preventing injection.

    Product
    OPTIRAY — OPTIRAY (IOVERSOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0138-2020·2019-10-16

    Guerbet Recalls Sodium Chloride Syringes Due to RFID Formatting Error

    Guerbet LLC is recalling 3,140 prefilled sodium chloride syringes because an RFID formatting error prevents the Optivantage injector from administering the product.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V732000·2019-10-15

    BMW Recalls 2019-2020 330i and Z4 Models for Engine Bearing Defect

    BMW is recalling 2019-2020 330i and 2019 Z4 vehicles because improperly installed counterbalance shaft bearings may loosen, causing severe engine damage and increasing crash risk.

    Product
    BMW — BMW 330I, Z4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V731000·2019-10-15

    GM Recalls 2020 Cadillac CT6 Vehicles for Tire Pressure Sensor Defect

    General Motors is recalling 2020 Cadillac CT6 vehicles with specific dealer-installed wheels because the tire pressure sensors use the wrong frequency, preventing low-pressure warnings.

    Product
    CADILLAC — CADILLAC CT6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V733000·2019-10-15

    Peterbilt 579 Recall for Incorrect Conspicuity Tape Placement

    PACCAR is recalling 2020 Peterbilt 579 sleeper trucks because conspicuity tape may be installed in the wrong location, reducing visibility to other drivers.

    Product
    PETERBILT — PETERBILT 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·097-2019·2019-10-14

    Kenosha Beef International Recalls Seasoned Beef Products Due to Metal Contamination

    Kenosha Beef International is recalling seasoned beef products that may contain metal shavings. The recall affects restaurant distribution nationwide.

    Product
    Kenosha Beef International, Ltd. — Kenosha Beef International Recalls Seasoned Beef Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V730000·2019-10-14

    E-One Recalls Emergency Vehicles Due to Starter Solenoid Circuit Defect

    E-One is recalling specific emergency vehicles because a missing diode in the starter solenoid circuit can damage the lock-out relay, potentially preventing the vehicle from starting.

    Product
    E-ONE — E-ONE TYPHOON, QUEST II, CYCLONE II, CHSH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V728000·2019-10-11

    Arcimoto Recalls 2019 FUV Motorcycles Due to Tie Rod Separation Risk

    Arcimoto is recalling 2019 FUV motorcycles because insufficient thread engagement in the tie rods could cause separation, leading to loss of steering and increased crash risk.

    Product
    ARCIMOTO — ARCIMOTO FUV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E069000·2019-10-11

    ASA Electronics Recalls Relay Modules for Voyager Rear Camera Displays

    ASA Electronics is recalling specific relay/capacitor modules used in Voyager rear camera displays. The modules may fail, causing loss of power to the display and increasing crash risk.

    Product
    BACK OVER PREVENTION: SENSING SYSTEM: CAMERA recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V727000·2019-10-11

    Forest River Recalls 2020 Shasta Trailers Due to Axle Hanger Defect

    Forest River is recalling 2020 Shasta Oasis SST30QB and SST31OK trailers because an incorrect axle hanger length may cause the axle to contact the chassis, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER SHASTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20009·2019-10-10

    Carrier Recalls Ductless Heat Pumps Due to Fire Hazard

    Carrier is recalling specific ductless heat pumps because a fan motor failure can cause overheating and fire. No injuries have been reported.

    Product
    Carrier- and Bryant-branded 1.5-ton multi-zone, 4-ton multi zone and 4-ton single-zone ductless heat pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E068000·2019-10-10

    Dorman Recalls Accelerator Pedal Assemblies for Acura and Honda Vehicles

    Dorman is recalling specific accelerator pedal assemblies for Acura and Honda vehicles because the rotating portion may bind, increasing crash risk.

    Product
    ACURA — ACURA, HONDA MDX, ACCORD, RIDGELINE, CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V722000·2019-10-10

    Western Star 4900 and 5700 Recall for Door Hinge Adhesive Failure

    Daimler Trucks North America is recalling 2017-2020 Western Star 4900 and 5700 trucks because the adhesive bond on side doors may fail, allowing doors to separate from the vehicle.

    Product
    WESTERN STAR — WESTERN STAR 4900, 5700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V718000·2019-10-10

    2020 Thomas Built Buses Minotour Recall for Seatbelt Warning Light Defect

    Daimler Trucks North America is recalling 2020 Thomas Built Buses Minotour school buses because the seatbelt-unfastened warning light may not illuminate for five seconds after ignition.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0046-2020·2019-10-09

    KRS Global Biotechnology Recalls Ephedrine Sulfate Syringes Due to Sterility Concerns

    KRS Global Biotechnology is recalling 3,895 syringes of ephedrine sulfate due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    ePHEDrine Sulfate in 0.9% Sodium Chloride (PF), 50 mg/5 mL (10 mg/mL) 5 mL Fill in a 6 mL Syringe, Single Dose Syringe. KRS Global Biotechnology 791 Park of Commerce Blvd, Boca Raton, FL 33487. NDC 3321678375
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0112-2020·2019-10-09

    KRS Global Biotechnology Recalls Vitamin 5 B Vials Due to Sterility Concerns

    KRS Global Biotechnology is recalling 616 vials of Vitamin 5 B for IM use because the company cannot ensure the product is sterile.

    Product
    Vitamin 5 B, 30 mL Vial For IM Use, Rx Only, KRS Global Biotechnology 791 Park of Commerce Blvd, Boca Raton, FL 33487. NDC 3321674253
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0089-2020·2019-10-09

    FDA Recalls Phenylephrine IV Bags Due to Sterility Concerns

    KRS Global Biotechnology is recalling Phenylephrine HCl IV infusion bags because the company cannot ensure the product is sterile.

    Product
    PHENYephrine HCl in 0.9% Sodium Chloride (PF) (Contains Sulfites). 30 mg/250 mL (0.12 mg/mL), 250 mL Single-Dose Bag For IV Infusion Use, Rx Only, KRS Global Biotechnology 791 Park of Commerce Blvd, Boca Raton, FL 33487. NDC 3321678401
    Category
    Drug
    Distribution
    Distributed nationwide