The Recall Desk

State

New Hampshire product recalls

73,566 recalls have nationwide distribution and so reach New Hampshire. 4,477 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,477
Critical
606
Severe
1,045
Most recent
2026-10-21

Of the 4,477 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 1,045 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,477 recalls whose distribution notice names New Hampshire specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25226–25250 of 78043

  • HighFDA (Devices)·Z-2120-2021·2021-07-28

    Exactech Hip Implant Liners Recalled for Premature Wear Risk

    Exactech Connexion GXL acetabular polyethylene liners used in hip implants face premature wear risk in certain patient and implant configurations. Consult your orthopedic surgeon if you have this device.

    Product
    Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 132-22-XX, Novation GXL Liner, G00, 22mm ID; and Novation GXL Liner, Lipped Ant, 28mm. Orthopedic hip implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2122-2021·2021-07-28

    Hip Implant Liners Recalled Due to Risk of Premature Wear

    Exactech Connexion GXL hip implant liners are being recalled due to a risk of edge-loading and premature prosthesis wear in patients with certain implant configurations and surgical positioning.

    Product
    Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 132-36-XX, Acumatch GXL 15 Degree Liner, 36mm, and Novation GXL Liner, Lipped Ant, 36mm; and Novation GXL Liner, Lipped, 36mm. Orthopedic hip implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2114-2021·2021-07-28

    Hip implant liners recalled due to risk of premature wear

    Exactech is recalling 89,050 hip implant liners due to risk of edge-loading and premature wear in specific patient and surgical configurations affecting a subset of patients.

    Product
    Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 104-36-XX, MCS +5GXL Liner 5/15 DEG and MCS GXL Liner 5/15 DEG. Orthopedic hip implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2098-2021·2021-07-28

    SoftCytogenetics Software Recalled for Incorrect Test Result Transmission

    Soft Computer Consultants, Inc. is recalling SoftCytogenetics software (versions 4.1.11.20, 4.1.12.11, 4.1.15.6) distributed in CA, FL, MN, and NJ because it produces incorrect results for retested specimens that are transmitted to clinical information systems.

    Product
    SoftCytogenetics
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2094-2021·2021-07-28

    Infant Heel Warmer Units Recalled for Rupture and Chemical Splashing Risk

    Cardinal Health is recalling 926,425 infant heel warmers (SKU MH00002T) due to reports of pack rupture or leaking during activation. The heated liquid may splash into a user's eyes or onto an infant, potentially causing rash, burn, or inflammation.

    Product
    Infant Heel Warmer with Attachment Tab, Nonsterile, Active Product SKU MH00002T The infant heel warmer is activated at the point of care by squeezing the pouch. This mixes the substrates inside the pouch causing an exothermic chemical reaction, warming the pouch, which is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2121-2021·2021-07-28

    Exactech GXL Acetabular Hip Implant Liners Recalled for Premature Wear Risk

    Exactech, Inc. is recalling 89,050 Connexion GXL and Novation GXL acetabular hip implant liners due to risk of edge-loading and premature prosthesis wear in certain patients. The risk depends on implant configuration and surgical positioning.

    Product
    Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 132-28-XX, Acumatch GXL 15 Degree Liner, 28mm; Novation GXL Liner, G0, 28mm ID; Novation GXL Liner, Lipped Ant, 28mm; and Novation GXL Liner, Lipped, 28mm. Orthopedic hip…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2081-2021·2021-07-28

    Moderna COVID-19 Vaccine Administration Kits Recalled for Unsuitable Syringes

    McKesson is recalling 53,388 Moderna COVID-19 vaccine administration kits due to unsuitable 3mL syringes included in the kits. The affected kits were distributed May 4-24, 2021, and should not be used for vaccine administration.

    Product
    ANCILLARY ADULT 140-DOSE CONVENIENCE KIT, ITEM #1189482, for the administration of the Moderna COVID-19 vaccine convenience kit for the administration of the COVID-19 vaccine
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2101-2021·2021-07-28

    Stryker Cortoss Bone Augmentation Material Recalled for Temperature Storage Violation

    Stryker Spine recalled Cortoss Bone Augmentation Material due to a 12-hour temperature excursion at the distribution center that could have compromised product sterility and efficacy.

    Product
    Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21172·2021-07-28

    Birkenstock Kids' Mogami Sandals Recalled for Choking Hazard

    Birkenstock USA has recalled Kids' Mogami Sandals in sizes 24-28 because a plastic rivet can detach from the ankle strap, posing a choking hazard for young children. No injuries have been reported.

    Product
    Birkenstock Kids' Mogami Sandals Sizes 24-28
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2103-2021·2021-07-28

    Knee Prosthesis Recall: Packaging Mixup May Cause Wrong Size Implantation

    Encore Medical recalls DJO Surgical EMPOWR 3D knee prosthetic components because packaging labels may not match the product inside, risking implantation of incorrect prosthesis sizes.

    Product
    DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus, REF: 341-12-711, Left Sz. 11 12mm, CE0086, Sterile H2O2, UDI: (01)00888912166980
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2100-2021·2021-07-28

    Cortoss Bone Augmentation Material Recalled Due to Storage Temperature Excursion

    Stryker Spine is recalling 559 units of Cortoss Bone Augmentation Material 5cc Cartridges due to a 12-hour temperature excursion at the distribution center. The affected lot may not meet required storage conditions.

    Product
    Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Number 2101-0005, GTIN 00808232000962
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2133-2021·2021-07-28

    Hip implant acetabular liners recalled for edge-loading and premature wear

    Exactech Connexion GXL acetabular polyethylene liners for hip implants are recalled due to risk of edge-loading and premature wear in certain patient configurations and implant positions. Approximately 89,050 units distributed nationwide are affected.

    Product
    Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 132-32-XX, Acumatch GXL 15 Degree Liner, 32mm; Novation GXL Liner, Lipped Ant, 32mm; and Novation GXL Liner, Lipped, 32mm. Orthopedic hip implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2105-2021·2021-07-28

    Cell Marque Rabbit Monoclonal Antibody Distributed Without FDA Clearance

    Cell Marque recalled 41 kits of a rabbit monoclonal antibody product distributed for in-vitro diagnostic use without required FDA clearance. The product was distributed in 16 US states.

    Product
    Cell Marque, RabMAb,CD17, c-kit (YR145) Rabbit Monoclonal Primary Antibody, REF: 117R-18, IVD, CE, GTIN: 00841683123798
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Drugs)·D-0689-2021·2021-07-28

    Erythromycin Topical Solution 2% Recalled for Failed Impurities Specifications

    Teligent Pharma, Inc. is recalling Erythromycin Topical Solution USP 2% (60 mL, Lot 14180) distributed nationwide because it failed impurities and degradation specifications.

    Product
    Erythromycin Topical Solution USP, 2% 60 mL, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310, NDC 52565-027-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2108-2021·2021-07-28

    Mindray battery cradle may prevent monitor from powering on

    Mindray is recalling the 3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 and TM80 Telepack physiological monitors. The cradle may prevent the monitor from powering on. Approximately 804 units were distributed in the US and Canada.

    Product
    3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 Telepack (Model Number 115-047566-00 /115-060044-00) and TM80 Telepack (Model Number 115-047565-00 / 120-018867-00). Used with physiological data monitor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0690-2021·2021-07-28

    Erythromycin Topical Gel 2% Recalled Due to Failed Impurity Specifications

    Teligent Pharma, Inc. is recalling Erythromycin Topical Gel 2% due to failed impurities and degradation specifications. The recall affects approximately 22,824 tubes distributed nationwide.

    Product
    Erythromycin Topical Gel, 2%, Net Wt. (a) 30 g,(NDC 52565-033-30) (b) 60 g,(NDC 52565-033-60) Rx Only, Manufactured by: Teligent Pharma, Inc. , Buena, NJ 08310,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V574000·2021-07-27

    Mack Recalls 2022 MD Trucks Due to Loose Front Suspension Bolts

    Mack Trucks is recalling 2022 MD trucks because loose front suspension bolts may detach, potentially causing loss of vehicle control and increasing crash risk.

    Product
    MACK — MACK MD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V573000·2021-07-27

    Mack Trucks Recalls 2021 LR, Granite, and TE Models for Brake Defect

    Mack Trucks is recalling 2021 LR, Granite, and TE vehicles because incorrect rear brake cams may cause inoperative rear axle brakes, increasing crash risk.

    Product
    MACK — MACK LR, GRANITE (GR), TE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21768·2021-07-27

    Oculus Quest 2 Removable Foam Facial Interfaces Due to Skin Irritation Risk

    Facebook Technologies is recalling about 4 million removable foam facial interfaces for Oculus Quest 2 virtual reality headsets because the foam can cause facial skin irritation and reactions. Consumers should stop using affected interfaces and contact the manufacturer for a free silicone replacement.

    Product
    Removable Foam Facial Interfaces for Oculus Quest 2 Virtual Reality Headsets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V571000·2021-07-27

    Newmar Recreational Vehicles Recalled for Window Adhesive Failure

    Newmar is recalling select 2018-2021 recreational vehicles due to potential window adhesive failure. The vent portion of affected windows may detach, increasing crash and injury risk.

    Product
    NEWMAR — NEWMAR BAY STAR, NEW AIRE, LONDON AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V568000·2021-07-26

    Eclipse Recalls 2020-2021 Trailers Due to Gas Leak Risk

    Eclipse is recalling 2020-2021 Attitude, Stellar, and Iconic trailers because a stove bolt may be overtightened, damaging the seal and causing a gas leak.

    Product
    ECLIPSE — ECLIPSE ATTITUDE, ICONIC, STELLAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V566000·2021-07-26

    2021–2022 Spartan K2 RV Chassis Fuel Leak Recall

    Shyft Group is recalling certain 2021–2022 Spartan K2 RV Chassis vehicles with Cummins L9 Diesel Engines due to fuel leaks from pressurized hoses. The leak may increase fire risk if an ignition source is present.

    Product
    SPARTAN — SPARTAN K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V567000·2021-07-26

    Marion Body Works Recalls Spartan Fire Emergency Vehicles for Pump Defect

    Marion Body Works is recalling 2009-2021 Spartan Fire Gladiator and MetroStar emergency vehicles because a corroded solenoid may cause loss of water pressure.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V569000·2021-07-26

    2021 Audi E-Tron recalled for brake booster defect

    Volkswagen is recalling certain 2021 Audi E-Tron models due to improperly welded brake boosters that may separate, reducing braking assistance and stability control.

    Product
    AUDI — AUDI E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide