The Recall Desk

State

New Hampshire product recalls

73,388 recalls have nationwide distribution and so reach New Hampshire. 4,472 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,472
Critical
606
Severe
1,042
Most recent
2026-09-23

Of the 4,472 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 1,042 (23%) are Severe.

These figures cover only the 4,472 recalls whose distribution notice names New Hampshire specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21201–21225 of 77860

  • SevereFDA (Food)·F-1126-2022·2022-06-08

    JIF Crunchy Peanut Butter Recall: Potential Salmonella Contamination

    The JM Smucker Company is recalling JIF Crunchy Peanut Butter (40 oz) due to potential Salmonella contamination. Affected products have lot codes 1274425 or 2140425 with best-by dates from October 1, 2023 to May 20, 2024.

    Product
    JIF 40 OUNCE CRUNCHY PEANUT BUTTER
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1108-2022·2022-06-08

    Jif Crunchy Peanut Butter Recalled for Potential Salmonella Contamination

    The JM Smucker Company is recalling JIF Crunchy Peanut Butter in multiple package sizes due to potential Salmonella contamination. The recall affects 1,567,672 cases distributed nationwide.

    Product
    JIF CRUNCHY PEANUT BUTTER packaged in 500 gram, 1 kilogram, 16oz, 28oz, 40oz, 48oz packaged in twin pack 80oz and 96oz
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1115-2022·2022-06-08

    JIF Natural Creamy Peanut Butter Recalled for Salmonella Contamination

    The JM Smucker Company is recalling certain JIF Natural Creamy peanut butter products distributed nationwide due to potential Salmonella contamination. Consumers should not consume the affected products.

    Product
    JIF NATURAL CREAMY packaged as a twin pack in 80oz and 96oz packaged as a squeezable pouch in 13oz
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1110-2022·2022-06-08

    JIF Crunchy Peanut Butter Recalled for Potential Salmonella Contamination

    The FDA is recalling 750 cases of JIF 12 ounce Crunchy Peanut Butter International due to potential Salmonella contamination. Consumers should not consume affected products with the specified lot codes and Best By dates.

    Product
    JIF 12 OUNCE CRUNCHY PEANUT BUTTER INTERNATIONAL
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1123-2022·2022-06-08

    JIF Peanut Butter Recalled for Potential Salmonella Contamination

    JIF 454 gram crunchy peanut butter from specific lot codes is being recalled due to potential Salmonella contamination. Affected products were distributed nationwide.

    Product
    JIF 454 GRAM CRUNCHY PEANUT BUTTER MEXICO
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1119-2022·2022-06-08

    JIF Natural Creamy Peanut Butter with Honey Recalled for Salmonella Risk

    The JM Smucker Company is recalling JIF 16 Ounce Natural Creamy Peanut Butter with Honey due to potential Salmonella contamination. The affected product was distributed across all U.S. states.

    Product
    JIF 16 OUNCE NATURAL CREAMY PEANUT BUTTER HONEY
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1122-2022·2022-06-08

    JIF Creamy Peanut Butter Recalled for Potential Salmonella Contamination

    The JM Smucker Company is recalling 20,021 cases of JIF 340-gram Creamy Peanut Butter due to potential Salmonella contamination. Affected products distributed nationwide should not be consumed; consumers should discard or return them.

    Product
    JIF 340 GRAM CREAMY PEANUT BUTTER MEXICO
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1127-2022·2022-06-08

    JIF Light Creamy Peanut Butter recalled for potential Salmonella contamination

    The JM Smucker Company is recalling JIF Light Creamy Peanut Butter due to potential Salmonella contamination. Affected products were distributed nationwide; consumers should verify lot codes and best-by dates and refrain from consuming the product.

    Product
    JIF LIGHT CREAMY PEANUT BUTTER packaged in 500 gram and 1 kilogram
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1114-2022·2022-06-08

    JIF Natural Creamy Peanut Butter recalled for potential Salmonella contamination

    The JM Smucker Company is recalling JIF Natural Creamy Peanut Butter in multiple package sizes due to potential Salmonella contamination. The recall affects 553,007 cases distributed nationwide.

    Product
    JIF NATURAL CREAMY PEANUT BUTTER packaged in 16oz, 28oz, 40oz, 48oz
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1113-2022·2022-06-08

    JIF 40 Ounce Natural Honey Recalled Due to Salmonella

    The JM Smucker Company is recalling JIF 40 Ounce Natural Honey due to potential Salmonella contamination. Affected products have lot codes 1274425 or 2140425 with best-by dates from October 2022 to May 2023.

    Product
    JIF 40 OUNCE NATURAL HONEY
    Category
    Food
    Distribution
    49 states
  • SevereNHTSA·22V405000·2022-06-08

    Commercial trucks recalled for defective steering gears

    Daimler Trucks is recalling 2022-2023 Freightliner MT45, MT45G, and Cascadia trucks because steering gears may have been incorrectly assembled and could fracture, causing loss of steering control.

    Product
    FCCC — FCCC, FREIGHTLINER MT45G, MT45, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1121-2022·2022-06-08

    JIF Creamy Peanut Butter To Go Recalled Due to Salmonella Risk

    The JM Smucker Company is recalling JIF 1.5 oz and 31.25 gram Creamy Peanut Butter To Go packages due to potential Salmonella contamination. These products were distributed to all 50 states.

    Product
    JIF 1.5 oz and 31.25 gram CREAMY PEANUT BUTTER TO GO packaged in 3, 8, 36, and 96 count cases
    Category
    Food
    Distribution
    49 states
  • HighFDA (Devices)·Z-1216-2022·2022-06-08

    Ratcheting Screwdriver Handle in Surgical Kit Unable to Meet Sterilization Requirements

    Tornier's Ratcheting Screwdriver Handle in the Aequalis Perform Reversed kit cannot meet sterilization requirements when sterilized per instructions in an Aesculap container. The company is recalling 1066 units distributed nationwide.

    Product
    Ratcheting Screwdriver Handle, provided in the Aequalis Perform Reversed kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1215-2022·2022-06-08

    BD Anti-Kappa PE Flow Cytometry Reagent May Show Inaccurate Results

    Becton Dickinson is recalling 199 units of BD Anti-Kappa PE flow cytometry reagent because samples may exhibit uncharacteristic flow profiles that could affect test accuracy.

    Product
    BD Anti-Kappa PE (Cat. No. 346587) is an analyte specific reagent for the Anti-Kappa antibody, which specifically recognizes the kappa light chains of human immunoglobulins. Anti-Kappa is used for in vitro identification of cells expressing the kappa light chains using flow…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1166-2022·2022-06-08

    FDA Recalls CVC Dressing Change Kit Due to Manufacturing Validation Uncertainty

    Busse Hospital Disposables is recalling CVC Dressing Change Kits nationwide due to uncertainty about test method validation during manufacturing. Affected swab products may not have been adequately validated for sterility and efficacy.

    Product
    CVC Dressing Change Kit Catalog Number: 2491R1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0966-2022·2022-06-08

    Phenylephrine HCl Injection recalled for lack of sterility assurance

    Nephron Sterile Compounding Center is recalling Phenylephrine HCl Injection syringes nationwide due to lack of assurance of sterility affecting 76,860 units.

    Product
    Phenylephrine HCl Injection, USP, 0.8 mg/10 mL (80 mcg/mL), 10 mL Pre-Filled Syringes, 5 x 10 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-956-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1169-2022·2022-06-08

    Epidural Tray Recalled Due to Manufacturing Validation Uncertainty

    Busse Hospital Disposables recalls approximately 425 units of its Single Shot Epidural Tray nationwide due to inadequate validation of manufacturing test methods for swab components.

    Product
    Single Shot Epidural Tray Catalog Number: 6183R1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1210-2022·2022-06-08

    Surgical Instrument Seal Defect Recall: da Vinci Energy SynchroSeal

    Intuitive Surgical recalls da Vinci Energy SynchroSeal surgical instruments due to potential seal failure. Excessive tissue in the instrument jaws can result in insufficient sealing.

    Product
    DAVINCI | Energy SynchroSeal da Vinci X' da Vinci Xi', Single Use Instrument 8mm, REF 480440
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0953-2022·2022-06-08

    Nephron Epinephrine Injection Recalled for Lack of Sterility Assurance

    Nephron Sterile Compounding Center is recalling 134,415 pre-filled syringes of Epinephrine Injection due to lack of assurance of sterility. Affected lots were distributed nationwide; patients and providers should contact their healthcare provider.

    Product
    Epinephrine Injection, USP, 1 mg/10 mL (100 mcg/mL), 10 mL Pre-Filled Syringe, 5 x 10 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-925-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1175-2022·2022-06-08

    Swab and Swabstick Drug Products Recalled for Manufacturing Validation Uncertainty

    Busse Convenience kits containing swab/swabstick drug products manufactured by Professional Disposables International are being recalled due to uncertainty about manufacturing test method validation.

    Product
    Joint Injection Tray Catalog Number: 8561R1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1154-2022·2022-06-08

    Swab and Swabstick Drug Products Recalled for Inadequate Manufacturing Validation

    Busse Convenience kits containing swab/swabstick drug products manufactured by Professional Disposables International (PDI) have been recalled due to uncertainty regarding the adequacy of manufacturing test method validation.

    Product
    Universal Tray Catalog 1567
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0961-2022·2022-06-08

    Injectable Labetalol HCl Syringes Recalled for Lack of Sterility Assurance

    Nephron Sterile Compounding Center has recalled 115,640 units of Labetalol HCl Injection due to lack of assurance of sterility. The affected product was distributed nationwide.

    Product
    Labetalol HCl Injection, USP, 20 mg/4 mL (5 mg/mL), Preservative Free, 4 mL Pre-Filled Syringe, 5 x 4 mL Pre-Filled Syringes, 6 x 5 Syringe Carton, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-946-04
    Category
    Drug
    Distribution
    Distributed nationwide