The Recall Desk

State

New Hampshire product recalls

73,718 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.

These figures cover only the 4,482 recalls whose distribution notice names New Hampshire specifically. The 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29651–29675 of 78200

  • HighFDA (Food)·F-1064-2020·2020-07-22

    Fresh Express Fancy Greens Recalled for Possible Cyclospora Contamination

    Fresh Express is recalling Fancy Greens salad products due to a possible health risk from Cyclospora. Consumers should check their refrigerators for affected products.

    Product
    Fresh Express Fancy Greens 7 oz., UPC 071279232010, Romaine lettuce, green tango, radicchio & carrots
    Category
    Food
    Distribution
    32 states
  • HighFDA (Food)·F-1060-2020·2020-07-22

    Fresh Express Chopped Kit Poppyseed Recalled for Cyclospora Risk

    Fresh Express Incorporated is recalling Chopped Kit Poppyseed salads due to a possible health risk from Cyclospora.

    Product
    Fresh Express Chopped Kit Poppyseed 11.7 oz, UPC 071279309118, Red and green cabbage, green leaf lettuce, carrots & green onions
    Category
    Food
    Distribution
    32 states
  • HighFDA (Devices)·Z-2628-2020·2020-07-22

    Skeletal Kinetics Recalls SKAFFOLD FLOW Bone Void Filler Kits

    Skeletal Kinetics is recalling SKAFFOLD FLOW bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life, potentially increasing surgical time or causing incomplete bone formation.

    Product
    SKAFFOLD FLOW (MX) 5CC. Product Number: SKMX-FL05, UDI: 813845020894 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1100-2020·2020-07-22

    Fresh Express Recalls Hy-Vee Avocado Ranch Salad Due to Cyclospora Risk

    Fresh Express is recalling Hy-Vee Chopped Kit Avocado Ranch Salad products due to a possible health risk from Cyclospora.

    Product
    Hy-Vee Chopped Kit Avocado Ranch Salad 12.8 oz., UPC 075450247152, Green cabbage, romaine lettuce, carrots, cilantro & green onions
    Category
    Food
    Distribution
    32 states
  • HighFDA (Food)·F-1026-2020·2020-07-22

    Freshness Guaranteed Five Cheese Stuffed Shells Recalled for Listeria Risk

    Garland Ventures is recalling Freshness Guaranteed Five Cheese Stuffed Shells due to potential Listeria monocytogenes contamination.

    Product
    Freshness Guaranteed Five Cheese Stuffed Shells Traditional Italian Ricotta Filled Shells with Marinara Sauce 10.76 ounces UPC 7874235174
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2629-2020·2020-07-22

    Skeletal Kinetics Recalls SKAFFOLD FLOW Bone Void Filler Kits

    Skeletal Kinetics is recalling SKAFFOLD FLOW bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life, potentially increasing surgical time or causing bone formation issues.

    Product
    SKAFFOLD FLOW, 10CC. Product Number: SKMX-FL10, UDI: 813845020900 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1054-2020·2020-07-22

    Fresh Express 3 Color Deli Cole Slaw Recalled for Cyclospora Risk

    Fresh Express is recalling 14 oz 3 Color Deli Cole Slaw due to a possible health risk from Cyclospora. Consumers should check their refrigerators for affected products.

    Product
    Fresh Express America's Fresh 3 Color Deli Cole Slaw" 14 oz, UPC 071279123004, (Canada UPC) 0 71279 12302 8 , Green cabbage, carrots & red cabbage
    Category
    Food
    Distribution
    32 states
  • HighFDA (Devices)·Z-2634-2020·2020-07-22

    Skeletal Kinetics Recalls Craniosculpt Bone Void Filler Kits

    Skeletal Kinetics is recalling Craniosculpt bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.

    Product
    CRANIOSCULPT, CMF IMPACT, 5CC, Product Number: C-CMF5CC, UDI: 813845020948 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1102-2020·2020-07-22

    Fresh Express Southwest Salad Recalled for Cyclospora Risk

    Fresh Express is recalling Hy-Vee Chopped Kit Southwest Salad due to a possible health risk from Cyclospora. Consumers should not eat the product.

    Product
    Hy-Vee Chopped Kit Southwest Salad 13.4 oz., UPC 075450246698, Red & green cabbage, green leaf lettuce, carrots & green onions
    Category
    Food
    Distribution
    32 states
  • HighFDA (Food)·F-1085-2020·2020-07-22

    Fresh Express Recalls Giant Eagle Chopped BBQ Ranch Salad Kits

    Fresh Express is recalling Giant Eagle Chopped BBQ Ranch Salad Kits due to a possible health risk from Cyclospora contamination.

    Product
    Giant Eagle Chopped BBQ Ranch Salad Kit 11.3 oz., UPC 030034923303, Cabbage and lettuce, carrots, and green onion
    Category
    Food
    Distribution
    32 states
  • HighFDA (Food)·F-1123-2020·2020-07-22

    Fresh Express Marketside Chopped Salad Kit Recalled for Cyclospora Risk

    Fresh Express is recalling Marketside Chopped Salad Kits due to a possible health risk from Cyclospora. Consumers should not consume the affected products.

    Product
    Marketside Chopped Salad Kit Sunflower Bacon Crunch 13.8 oz., UPC 681131148344, Green & red cabbage, kale, romaine lettuce, green onions & carrots
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Drugs)·D-1388-2020·2020-07-22

    Akorn Recalls Proparacaine Hydrochloride Ophthalmic Solution Due to Chemical Contamination

    Akorn, Inc. is recalling Proparacaine Hydrochloride Ophthalmic Solution, 0.5%, due to chemical contamination from equipment cleaning residue.

    Product
    Proparacaine Hydrochloride Ophthalmic Solution, USP, 0.5%, 15 mL per dropper bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC 17478-263-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1390-2020·2020-07-22

    Preferred Pharmaceuticals Recalls Lidothol Patches Due to Missing Batch Records

    Preferred Pharmaceuticals is recalling Lidothol Patches because the contract manufacturer misplaced or lost batch records and test results.

    Product
    Lidothol Patch, Lidocaine 4.5% & Menthol 5%, In each patch: lidocaine 4.5% topical anesthetic, menthol 5% topical analgesic, Pkg Size 15 patches per box, Insurance NDC: 53225-1025-01, Mfg: Terrain Pharmaceuticals; Reno, NV, Prod # (NDC): 68788-7405-01, Preferred Pharmaceuticals…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2591-2020·2020-07-22

    Shimadzu Recalls Three Trinias DAP Meters for Tolerance Issues

    Shimadzu Medical Systems is recalling three Trinias DAP Meters because they were found to be outside of tolerance. The devices are used in interventional procedures.

    Product
    Trinias DAP Meter, a component of the Digital Anglo System Trinias contained within the DAR-9500f - Product Usage: It is intended to be used for interventional procedures, such as invasive cardiology, interventional radiology, and interventional neuroradiology.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2590-2020·2020-07-22

    DJO Nylatex Wraps Recalled for Missing Latex Warning Labels

    DJO, LLC is recalling Nylatex wraps used with Intelect and V-Sonic devices because they lack appropriate latex warning labels.

    Product
    This is an accessory to Intelect Advanced, Intelect Mobile, Intelect Neo, and V-Sonic devices. NYLATEX WRAP - Product Usage: are intended to be used based on the devices associated with them. Nylatex wraps are composed of nylon and natural rubber and are accessories used to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1389-2020·2020-07-22

    Keryx Recalls Auryxia Tablets Due to Manufacturing Process Deviations

    Keryx Biopharmaceuticals is recalling 59,820 bottles of Auryxia (ferric citrate) tablets because they were not manufactured in conformance with the FDA-approved process.

    Product
    AURYXIA — AURYXIA (FERRIC CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2638-2020·2020-07-22

    Neocis Dental Chairside Splints Recalled for Potential Mislabeling

    Neocis Inc. is recalling 70 units of Gen 2 Posterior Chairside Splints due to potential mislabeling. The affected products are used in dental implantation surgery.

    Product
    DRW-0739-02: Gen 2 Posterior Chairside Splint LRUL (lower right-upper left) - Product Usage: intended to provide assistance in both the planning (pre-operative) and the surgical (intra-operative) phases of dental implantation surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2637-2020·2020-07-22

    Neocis Dental Chairside Splints Recalled for Potential Mislabeling

    Neocis Inc. is recalling specific dental chairside splints because they may be mislabeled. The recall covers 70 units distributed nationwide.

    Product
    DRW-0739-01: Gen 2 Posterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intended to provide assistance in both the planning (pre-operative) and the surgical (intra-operative) phases of dental implantation surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2639-2020·2020-07-22

    Neocis Gen 2 Anterior Chairside Splint Recalled for Mislabeled Packaging

    Neocis Inc. is recalling 50 units of Gen 2 Anterior Chairside Splints due to potential mislabeling. The affected products are distributed nationwide.

    Product
    DRW-0742-01: Gen 2 Anterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intended to provide assistance in both the planning (pre-operative) and the surgical (intra-operative) phases of dental implantation surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1391-2020·2020-07-22

    Fresenius Kabi Recalls Fosaprepitant Injection Due to Labeling Error

    Fresenius Kabi USA, LLC is recalling 63,067 vials of Fosaprepitant for Injection because carton labels and product inserts incorrectly state the amount of the excipient edetate disodium (EDTA).

    Product
    FOSAPREPITANT — FOSAPREPITANT (FOSAPREPITANT)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2550-2020·2020-07-22

    Access Scientific Recalls Mislabeled Powerwand XL Maximum Barrier Kits

    Access Scientific LLC is recalling 1,710 Powerwand XL kits due to incorrect catheter length labels. The error may cause treatment delays or user annoyance.

    Product
    POWERWAND XL 4Fr 8cm Maximum Barrier Kit (Introducer with an Extended Dwell Catheter made of ChronoFlex C with BioGUARD Technology), Catalog No. 94108, Device UDI 00859821006773/Pacakge UDI 10859821006770 - Product Usage: Introducer with Extended Dwell Catheter is used to gain…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V421000·2020-07-21

    Newmar Recalls Motorhomes with Damaged Rear Power Distribution Modules

    Newmar is recalling specific 2016-2020 motorhomes because a damaged rear Power Distribution Module may cause exterior lights to stop working, increasing crash risk.

    Product
    NEWMAR — NEWMAR NEW AIRE, LONDON AIRE, ESSEX, VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V419000·2020-07-20

    2021 Thor Motor Coach motorhomes recalled for battery cable fire risk

    Thor Motor Coach is recalling 2021 motorhomes because an improperly secured battery cable may contact the exhaust manifold and pose a fire risk. Owners should contact Thor Motor Coach for a free inspection and repair.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH QUANTUM, CHATEAU, FREEDOM ELITE, DAYBREAK
    Category
    Vehicle
    Distribution
    Distributed nationwide