The Recall Desk

State

New Hampshire product recalls

72,966 recalls have nationwide distribution and so reach New Hampshire. 4,444 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,444
Critical
596
Severe
846
Most recent
2026-09-09

Of the 4,444 recalls naming New Hampshire we have scored against our rubric, 596 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 846 (19%) are Severe.

These figures cover only the 4,444 recalls whose distribution notice names New Hampshire specifically. The 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5676–5700 of 77410

  • HighNHTSA·25V535000·2025-08-21

    Trailer radio and speakers can overheat from a software error

    Aluminum Trailer Company is recalling certain 2023-2025 trailers because a software error may cause the radio and speakers to overheat, increasing the risk of fire.

    Product
    ATC — ATC RM550, PL500, ST450, RM450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V536000·2025-08-21

    Chevrolet Corvette refuelling spillage can reach an ignition source

    General Motors is recalling certain 2023-2026 Corvette vehicles with a left-side radiator/fan combination because excess fuel may spill into the filler pocket during refuelling and leak onto an ignition source.

    Product
    CHEVROLET — CHEVROLET CORVETTE CONVERTIBLE, CORVETTE COUPE, CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0544-2025·2025-08-20

    Reser's tuna salad containing pickle relish recalled for Listeria monocytogenes risk

    Reser's Tuna Salad in 5 lb foodservice tubs, the version containing pickle relish, is recalled for potential Listeria monocytogenes contamination from recalled breadcrumbs. 108 cases are affected.

    Product
    Reser's Tuna Salad, net wt. 5lb. Foodservice item. Product is packaged in white plastic tub and lid with sticker. Keep Refrigerated. This item contains ingredient Pickle Relish. Distributed by Reser's Fine Foods, Incl, Beaverton, OR. UPC on 5lb. TUB/Lid: 71117 11405 GTIN on Mas
    Category
    Food
    Distribution
    29 states
  • CriticalFDA (Devices)·Z-2290-2025·2025-08-20

    HeartMate mobile power unit cords recalled over locking feature that may disconnect

    Abbott is recalling 53 HeartMate Mobile Power Unit AC power cords, model 107760, because a misaligned V-Lock may not engage and can allow an unintended disconnect. The FDA classified this as Class I.

    Product
    Brand Name: HeartMate Product Name: Mobile Power Unit, AC Power Cord Model/Catalog Number: 107760 Software Version: N/A Product Description: The HeartMate 3" Left Ventricular Assist System (LVAS) is a set of equipment and materials that together comprise a medical device desi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0542-2025·2025-08-20

    Sysco foodservice tuna salad recalled over Listeria risk from recalled breadcrumbs

    Sysco Imperial Deluxe Tuna Salad in 5 lb foodservice tubs is recalled for potential Listeria monocytogenes contamination traced to recalled Newly Weds Foods breadcrumbs. 70 cases are affected.

    Product
    Sysco Imperial Deluxe Tuna Salad, Reorder #6526826, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic tub with printed white lid. Keep Refrigerated. Distributed by Sysco Corporation, Houston, TX 77077 UPC on 5lb. TUB: 74865 79721 GTIN on Master Case (2/
    Category
    Food
    Distribution
    29 states
  • CriticalFDA (Devices)·Z-2173-2025·2025-08-20

    Infusion pumps recalled over underinfusion when flow rate more than doubles

    Baxter is issuing an urgent correction for 36,705 Novum IQ large volume pumps because the pump may underinfuse when moving to a flow rate more than double the current one.

    Product
    Baxter Novum IQ Large Volume Pump, Product Code REF 40700BAXUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0545-2025·2025-08-20

    Molly's Kitchens tuna salad recalled for Listeria risk from recalled breadcrumbs

    Molly's Kitchens Tuna Salad in 5 lb foodservice tubs, distributed by US Foods, is recalled for potential Listeria monocytogenes contamination from recalled Newly Weds Foods breadcrumbs. 1,136 cases are affected.

    Product
    Molly's Kitchens Tuna Salad, item 794599, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic tub with printed white lid. Keep Refrigerated. Distributed by U.S. Foods, Inc, Rosemont, IL. UPC on 5lb. TUB/Lid: 58108 76447 GTIN on Master Case (2/5# per cas
    Category
    Food
    Distribution
    29 states
  • CriticalFDA (Devices)·Z-2273-2025·2025-08-20

    Carotid stent delivery systems recalled over resistance during withdrawal after deployment

    Certain batches of the Carotid WALLSTENT Monorail Endoprosthesis are being removed after complaints of greater than anticipated resistance withdrawing the delivery system. The most serious potential consequence is stroke.

    Product
    Carotid WALLSTENT Monorail Endoprosthesis Closed Cell Self-Expanding Stent, stent and stent delivery system. Material numbers: H7493915010240 CAROTID WALLSTENT MONORAIL 10.0-24; H7493915010310 CAROTID WALLSTENT MONORAIL 10.0-31; H749391506220 CAROTID WALLSTENT MONORAIL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2181-2025·2025-08-20

    Manual resuscitators recalled because blocked manometer port may disable pressure gauge

    Ambu is recalling 87,156 SPUR II adult resuscitators because the manometer port may be blocked, leaving the manometer non-functional. The FDA classified the action as Class I.

    Product
    Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator, Adult, Catalog Number: 523211000 2 SPUR II Adult Resuscitator w/Mercury Filter, Adult, Catalog Number: 523611051 3 SPUR II Adult Resuscitator, Single Patient Use Resuscitator, Adult, Catalog Number: 523611057 4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0543-2025·2025-08-20

    Sysco Classic tuna salad recalled over Listeria risk from recalled breadcrumbs

    Sysco Classic Tuna Salad in 5 lb foodservice tubs is recalled for potential Listeria monocytogenes contamination traced to recalled Newly Weds Foods breadcrumbs. 779 cases are affected.

    Product
    Sysco Classic Tuna Salad, Reorder #6724249, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic tub with printed lid. Keep Refrigerated. Distributed by Sysco Corporation, Houston, TX 77077 UPC on 5lb. Sysco TUB/Lid: 74865 80038 GTIN on Master Case (2/5#
    Category
    Food
    Distribution
    29 states
  • CriticalFDA (Food)·H-0540-2025·2025-08-20

    Reser's tuna salad without pickle relish recalled over Listeria contamination risk

    Reser's Tuna Salad in 5 lb foodservice tubs, the version without pickle relish, is recalled for potential Listeria monocytogenes contamination from recalled breadcrumbs. 173 cases are affected.

    Product
    Reser's Tuna Salad, net wt. 5lb. Foodservice item. Product is packaged in white plastic tub and lid with sticker. Keep Refrigerated. This item does not contain ingredient Pickle Relish. Distributed by Reser's Fine Foods, Beaverton, OR. UPC on 5lb. TUB: 71117 14138 GTIN on Maste
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Devices)·Z-2228-2025·2025-08-20

    DreamStation Auto BiPAP units may hold an incorrect device configuration

    DreamStation Auto BiPAP non-continuous ventilators are being recalled because the devices may possess a programming error resulting in an incorrect device configuration. 8 units are affected.

    Product
    DreamStation Auto BiPAP. Non-Continuous Ventilator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V533000·2025-08-20

    Mercedes steering coupling bolt may loosen from the steering rack

    Mercedes-Benz is recalling certain 2023-2026 EQE and GLC vehicles because the steering coupling bolt may have been improperly tightened, allowing the coupling to loosen from the steering rack.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQE 500 4MATIC, EQE 350 4MATIC, GLC 350 E 4MATIC, GLC 300 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2227-2025·2025-08-20

    DreamStation Auto CPAP units may hold an incorrect device configuration

    DreamStation Auto CPAP non-continuous ventilators are being recalled because the devices may possess a programming error resulting in an incorrect device configuration. 57 units are affected.

    Product
    DreamStation Auto CPAP. Non-Continuous Ventilator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2291-2025·2025-08-20

    HeartMate mobile power unit cords may disconnect from a misaligned lock

    HeartMate Mobile Power Units are being recalled because misaligned V-Lock features on the power cords prevent the locking mechanism engaging properly and may cause unintended disconnect. 604 units affected.

    Product
    Brand Name: HeartMate Product Name: Mobile Power Unit Model/Catalog Number: 107754 Software Version: N/A Product Description: The HeartMate 3" Left Ventricular Assist System (LVAS) is a set of equipment and materials that together comprise a medical device designed to provide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V532000·2025-08-20

    Aston Martin Recalls 2025 Vanquish for Brake Assist Software Defect

    Aston Martin is recalling 2025 Vanquish vehicles because a vacuum pump defect may cause loss of power brake assist, increasing stopping distance and crash risk.

    Product
    ASTON MARTIN — ASTON MARTIN VANQUISH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·028-2025·2025-08-20

    Sabrositos Hondurenos Recalls Meat Products Produced Without Federal Inspection

    Sabrositos Hondurenos, LLC is recalling approximately 32,000 pounds of meat products that were produced without federal inspection and bear false USDA marks.

    Product
    Sabrositos Hondurenos, LLC, Recalls Various Meat Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0539-2025·2025-08-20

    Signature Cafe tuna salad recalled over Listeria in recalled breadcrumbs

    Signature Cafe Premium Tuna Salad, 3 lb foodservice tubs, is being recalled because it contains Newly Weds Foods recalled Japanese style breadcrumbs, with potential Listeria monocytogenes contamination. 165 cases affected.

    Product
    Signature Cafe Premium Tuna Salad, net wt. 3lb (48oz). Foodservice item to be used by deli. Product is packaged in clear plastic tub with printed white lid. Keep Refrigerated. Distributed by Lucerne Foods, PO Box 99, Pleasanton, CA. UPC on 3lb. TUB: 71117 06036 GTIN on Mast
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Food)·H-0541-2025·2025-08-20

    Reser's gourmet tuna salad recalled over Listeria in recalled breadcrumbs

    Reser's Gourmet Tuna Salad, 5 lb foodservice tubs, is being recalled because it contains Newly Weds Foods recalled Japanese style breadcrumbs, with potential Listeria monocytogenes contamination. 240 cases affected.

    Product
    Reser's Gourmet Tuna Salad, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic tub with white lid with white sticker. Keep Refrigerated. Distributed by Reser's Fine Foods, Beaverton, OR. UPC on 5lb. TUB: 71117 85506 GTIN on Master Case (2/5# per case):
    Category
    Food
    Distribution
    29 states
  • HighFDA (Devices)·Z-2285-2025·2025-08-20

    Knee tibial insert catalog number 341-16-704 recalled for mislabeled size or side

    Enovis is recalling 18 EMPOWR 3D Knee tibial inserts, catalog number 341-16-704, lot 148T1057, because the implants carry incorrect size or side labeling.

    Product
    Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 4L 16MM, VE Model/Catalog Number: 341-16-704 Product Description: Enovis knee devices are intended for treatment of patients who are candidates for knee arthroplasty per the Indication for use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0585-2025·2025-08-20

    Lactated Ringer's containers may leak at a weld site

    Lactated Ringer's Injection USP in 1000 mL Excel containers is being recalled for lack of assurance of sterility because of the potential for fluid leakage at one of the weld sites. 74,088 containers affected.

    Product
    LACTATED RINGERS — LACTATED RINGERS (SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0588-2025·2025-08-20

    Carvedilol 25 mg tablets recalled over nitrosamine impurity above FDA limit

    Glenmark Carvedilol Tablets USP, 25 mg, in 500-tablet cartons are recalled nationwide after N-Nitroso Carvedilol Impurity-1 was found above the FDA-recommended limit. 14,976 bottles are affected.

    Product
    CARVEDILOL — CARVEDILOL (CARVEDILOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0469-2025·2025-08-20

    Helados Mexico variety paletas list cream without declaring milk as source

    Helados Mexico Minis Variety Paletas 12-count are being recalled because the label includes the ingredient cream but does not include milk as the source. 42,488 units are affected.

    Product
    Helados Mexico Minis Variety Paletas 12-Count 18oz UPC:6-82082-61215-1
    Category
    Food
    Distribution
    Distributed nationwide