The Recall Desk

State

New Hampshire product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37076–37100 of 78289

  • HighNHTSA·19V133000·2019-02-27

    Triumph Recalls Motorcycles Due to Clutch Cable Wiring Damage Risk

    Triumph is recalling specific 2016-2019 motorcycles because the clutch cable may damage wiring, potentially causing electrical failures or engine stalling.

    Product
    TRIUMPH — TRIUMPH SCRAMBLER, STREET TWIN, BONNEVILLE T120 BLACK, STREET CUP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0938-2019·2019-02-27

    Century Snacks Recalls Praline Pecans Due to Mispackaging

    Century Snacks LLC is recalling 25 packages of Praline Pecans because they were mispackaged with Praline Almonds. The error creates an undeclared allergen risk for consumers with nut allergies.

    Product
    Snak Club Praline Pecans Made With Cane Sugar NET Wt. 2.25 oz (64 g) Produced By: Century Snack Commerce, CA 90040 centurysnacks.com
    Category
    Food
    Distribution
    6 states
  • HighNHTSA·19V134000·2019-02-27

    Lexus Recalls 2018 LS Models for Run-Flat Tire Defect

    Toyota is recalling 2018 Lexus LS vehicles because run-flat tires may have cracked reinforcement layers, potentially causing tread separation and affecting vehicle stability.

    Product
    LEXUS — LEXUS LS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V140000·2019-02-27

    Midway Recalls One 2016 Freightliner Sprinter 3500 Wheelchair Lift Vehicle

    Midway Specialty Vehicles is recalling one 2016 Freightliner Sprinter 3500 because a wheelchair lift component may fail, causing the platform to rise too high and increasing injury risk.

    Product
    FREIGHTLINER — FREIGHTLINER SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0848-2019·2019-02-27

    Ortho-Clinical Diagnostics Recalls VITROS VALP Reagent Packs Due to Negative Bias

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products VALP Reagent Packs because they may produce negative bias results when measuring valproic acid.

    Product
    VITROS Chemistry Products VALP Reagent Pack. For in vitro diagnostic use only. CATALOG #(s): 6801710 INTENDED USE: For in vitro diagnostic use only. VITROS Chemistry Products VALP Reagent is used on the VITROS 5,1 FS Chemistry System, the VITROS 4600 Chemistry System and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0852-2019·2019-02-27

    Boston Scientific Recalls Mislabelled Stingray Guidewires for Coronary Procedures

    Boston Scientific is recalling 49 Stingray Guidewires that are 185cm but incorrectly labeled as 300cm. The mislabeling could lead to improper use during angioplasty procedures.

    Product
    Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other intravascular devices during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0513-2019·2019-02-27

    Lupin Recalls Lovastatin Tablets Due to CGMP Deviations

    Lupin Pharmaceuticals is recalling Lovastatin 40 mg tablets because the drug substance used was out of specification for impurity results.

    Product
    LOVASTATIN — LOVASTATIN (LOVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0844-2019·2019-02-27

    Ortho Vitros Myoglobin Calibrators Recalled for Stability Issues

    Ortho Clinical Diagnostics is recalling Vitros Myoglobin Calibrators due to a stability issue that may cause calibration failures or atypical quality control results.

    Product
    Vitros Myoglobin Calibrators, Product Code 6801043 For use in the calibration of the VITROS ECi/ECiQ Immunodiagnostic Systems, the VITROS 3600 Immunodiagnostic System and the VITROS 5600 Integrated System for the quantitative measurement of myoglobin in human serum and plasma
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0499-2019·2019-02-27

    Advanced Pharma Recalls Oxytocin Injectable Solution Due to Superpotency

    Advanced Pharma Inc. is recalling Oxytocin 30 Units Injectable Solution because the product may contain higher concentrations than labeled.

    Product
    Oxytocin 30 Units added to NS 500 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 503 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-706-50.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0511-2019·2019-02-27

    Akorn Recalls Moisturizing Lubricant Eye Drops Due to Stability Failure

    Akorn Inc is recalling specific lots of Moisturizing Lubricant Eye Drops because they failed stability specifications for Sodium Perborate.

    Product
    Moisturizing Lubricant Eye Drops, 0.25% Sodium Carboxymethylcellulose, 0.5 Fl OZ (15mL) Distributed by: Walgreen Co, 200 Wilmont Rd Deerfield IL 60015 NDC 00363-9651-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0842-2019·2019-02-27

    Smiths Medical Recalls Arterial Blood Sampling Kits with Povidone Iodine Pads

    Smiths Medical ASD Inc. is recalling arterial blood sampling kits because the included povidone iodine prep pads may not maintain potency through their expiration dates.

    Product
    Aplicare Povidone Iodine Prep Pads packaged within Portex Pro-Vent Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes, models 4589P-1, 4591EG-1, 4591P-1, 4599P-1, 4611LH, 4611P-1, 4620EG-1, 4620P-1, 4640LH, 4640P-1, 4649P-1, 4660EG-1, 4660P-1…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0515-2019·2019-02-27

    Akorn Recalls Clobetasol Propionate Cream Due to Preservative Stability Failure

    Akorn Inc. is recalling specific lots of Clobetasol Propionate Emollient Cream 0.05% because stability testing revealed out-of-specification preservative levels.

    Product
    Clobetasol Propionate Emollient Cream 0.05%, a) 30 gram (NDC 50383-270-30) and b) 60 gram (NDC 50383-270-60) tubes, Rx only. Manufacturer: Akorn Inc. 369 Bayview Ave., Amityville, NY 117701.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0498-2019·2019-02-27

    Advanced Pharma Recalls Oxytocin Injectable Solution Due to Superpotency

    Advanced Pharma Inc. is recalling 672 bags of Oxytocin 20 Units Injectable Solution because the product may contain higher concentrations than labeled.

    Product
    Oxytocin 20 Units added to NS 1000 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 1002 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-703-99.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0843-2019·2019-02-27

    Smiths Medical Recalls Arterial Blood Sampling Kits Due to Iodine Potency

    Smiths Medical ASD Inc. is recalling Portex Pulsator Arterial Blood Sampling Kits because the included povidone iodine prep pads may not maintain potency through their expiration dates.

    Product
    Aplicare Povidone Iodine Prep Pads packaged within Portex Pulsator Arterial Blood Sampling Kit with Liquid Sodium Heparin, models 4037NP-1, 4039-1, 4039EG-1, 4044EG-1, 4044P-1, 4057NP-1, 4067NP-1, 4077EG-1, 4077NP-1, 4084P-1, G1193, G1374, G1585, G1589, G1598, G1621, and G1806.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0512-2019·2019-02-27

    Perrigo Recalls Ciclopirox Shampoo Due to Stability Testing Failures

    Perrigo New York, Inc. is recalling specific lots of Ciclopirox shampoo 1% because stability testing revealed out-of-specification related substances.

    Product
    CICLOPIROX — CICLOPIROX (CICLOPIROX)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0497-2019·2019-02-27

    Advanced Pharma Recalls Oxytocin Injectable Solution Due to Superpotent Drug Concerns

    Advanced Pharma Inc. is recalling 12 bags of Oxytocin 10 Units Injectable Solution because the product may contain higher concentrations than labeled.

    Product
    Oxytocin 10 Units added to NS 1000 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 1001 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-730-99.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0514-2019·2019-02-27

    Mometasone Furoate Cream Recalled for NDC Typographical Error

    ACP Nimble Buyer, Inc. is recalling Mometasone Furoate Cream due to a typographical error in the National Drug Code (NDC) on the label.

    Product
    Mometasone Furoate Cream, 0.1%, 45 g tube, Rx Only, Manufactured by: G&W Laboratories, Inc. South Plainfield, NJ 07080, NDC 0713-0726-37
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V122000·2019-02-26

    International LT and Prostar Trucks Recalled for Exhaust Bracket Crack Risk

    Navistar is recalling 2016-2020 International LT and 2017-2018 Prostar trucks because a cracked exhaust bracket could cause the tailpipe to detach, creating a road hazard.

    Product
    INTERNATIONAL — INTERNATIONAL PROSTAR, LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·022-2019·2019-02-26

    Sahlen Recalls Deli Ham Due to Possible Plastic Contamination

    Sahlen Packing Company is recalling approximately 13,224 pounds of ready-to-eat deli ham products that may contain plastic. The products were distributed to retail locations in six northeastern states.

    Product
    Sahlen Packing Company, Inc. — Sahlen Packing Company, Inc. Recalls Ready-To-Eat Deli Meat Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    6 states
  • HighNHTSA·19V132000·2019-02-26

    Mercedes-Benz Recalls GLA 250 Vehicles for Rear Seat Covering Defect

    Mercedes-Benz is recalling 2018-2019 GLA 250 vehicles because an incorrect rear seat covering may hide the center child seat anchor point, increasing crash injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V131000·2019-02-26

    Mercedes-Benz Recalls 2018 CLA 250 Vehicles for Tail Light Defect

    Mercedes-Benz is recalling 2018 CLA 250 and CLA 250 4MATIC vehicles because tail and side marker lights may flicker or fail, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V130000·2019-02-26

    Mercedes-Benz Recalls C and E Class Vehicles for Seatback Lock Defect

    Mercedes-Benz is recalling 2017-2018 C and E Class vehicles because front seatbacks may not lock properly, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300, E 400, AMG C43, AMG C63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19071·2019-02-26

    JumpSport Recalls Mini Trampolines Due to Frame Injury Hazard

    JumpSport is recalling about 11,300 half-fold fitness mini-trampolines because the folding frame can forcefully hit users, causing cuts, bruises, and dental injuries.

    Product
    JumpSport® half-fold fitness mini-trampolines
    Category
    Consumer Product
    Distribution
    Distributed nationwide