The Recall Desk

State

New Hampshire product recalls

73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26876–26900 of 78053

  • HighFDA (Devices)·Z-1116-2021·2021-02-24

    Medtronic Recalls Cerebrospinal Fluid Valves Due to Radiopaque Marking Issues

    Medtronic Neurosurgery is recalling 22,528 units of STRATA II cerebrospinal fluid valves and shunts worldwide because radiopaque markings may vary in visibility under imaging.

    Product
    Medtronic Cerebro Spinal Fluid Flow Control Valves and Shunts. STRATA II Valves and Shunts for the following CFNs: 27739 - SHUNT 27739 STRATA NSC SNAP SML 120CM, 27740 - SHUNT 27740 STRATA NSC SNAP REG 120CM, 27812 - VALVE 27812 STRATA II SM EXTRACTED, 27814 - SHUNT…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1125-2021·2021-02-24

    Confirm Biosciences Recalls Healgen COVID-19 Rapid Test Cassettes

    Confirm Biosciences is recalling Healgen COVID-19 Rapid Test Cassettes because they were distributed to non-certified labs and not validated for fingerstick use.

    Product
    Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCC)V-402a - Product Usage: is a lateral flow immunoassay intended for the qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV- 2 in human venous whole blood, plasma from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1128-2021·2021-02-24

    Cairn Diagnostics Recalls 13C-Spirulina Gastric Emptying Breath Test Kits

    Cairn Diagnostics is recalling 103 kits of the 13C-Spirulina Gastric Emptying Breath Test due to a potential for false negative diagnoses of gastroparesis.

    Product
    13C-Spirulina Gastric Emptying Breath Test (GEBT) - Product Usage: intended for use in the measurement of the rate of gastric emptying of solids and as an aid in the diagnosis of delayed gastric emptying (gastroparesis) in adult humans who are symptomatic for gastroparesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0257-2021·2021-02-24

    DLC Laboratories Recalls Sulfur Ointment Jars Due to Labeling Error

    DLC Laboratories is recalling 86,297 jars of Sulfur Ointment 10% because English labels for Camphor were incorrectly applied to the product.

    Product
    Sulfur Ointment 10%, Pomada de Azufre, 2.6 OZ (73.7g) jar; Manufactured by/ Fabricado por: De La Cruz Products, A Division of DLC Laboratories, Inc. Paramount, CA 9023 USA; UPC 024286150426
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0264-2021·2021-02-24

    Ascend Recalls Cephalexin Oral Suspension Due to CGMP Deviations

    Ascend Laboratories LLC is recalling Cephalexin for Oral Suspension due to CGMP deviations involving unidentified impurities.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0260-2021·2021-02-24

    Auryxia Tablets Recalled for Failed Dissolution Specifications

    Akebia Therapeutics is recalling Auryxia (ferric citrate) tablets because they failed to meet dissolution specifications.

    Product
    Auryxia (ferric citrate) tablets, 210 mg*, 200 tablets bottle, RX ONLY, Manufactured for and distributed by: KERYX BIOPHARMACEUTICALS, INC., 245 First Street, Suite 1400, Cambridge, MA 02142, USA, NDC 59922-0631-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0263-2021·2021-02-24

    Ascend Recalls Cephalexin Oral Suspension Due to Impurity Levels

    Ascend Laboratories is recalling Cephalexin for Oral Suspension because unidentified impurities were found at higher levels than allowed.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1115-2021·2021-02-24

    Medtronic Delta CSF Valves Recalled for Radiopaque Marking Visibility Issues

    Medtronic is recalling Delta CSF flow control valves because radiopaque markings may not be clearly visible under X-ray imaging.

    Product
    Medtronic Delta CSF (Cerebro Spinal Fluid) -Flow Control Valves for the following CFNs/REF numbers: 24048 - VALVE 24048 DELTA RGL PL 0.5, 24053 - CHAMBER 24053 DELTA, 24147 - VALVE 24147 DELTA SML PL0.5, 25121-1 - ASSY 25121-1 DELTA SML SNAP PERIT 120, 25121-5 - ASSY…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1117-2021·2021-02-24

    Medtronic CSF-Flow Control Valves Recalled for Radiopaque Marking Visibility Issues

    Medtronic Neurosurgery is recalling 20,817 CSF-Flow Control Valves worldwide due to potential variation in radiopaque marking visibility under radiographic imaging.

    Product
    Medtronic PS Medical Cerebro Spinal Fluid (CSF)-Flow Control Valves for the following CFNs: 22011 L- SHUNT 22011 L INTL ONLY ULTRA SM LOW 22011 LL - SHUNT 22011 LL INTL ONLY ULTRA SM L-L 22011 M - SHUNT 22011 M INTL ONLY ULTRA SM MED 22017 B-L - SHUNT 22017 B-L ASSY US…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1127-2021·2021-02-24

    Sky Medical SARS-CoV-2 Rapid Test Kits Recalled for Lack of Emergency Use Authorization

    Sky Medical Supplies and Equipments LLC is recalling 10,000 SARS-CoV-2 rapid test kits distributed in Florida and Peru because they were sold without FDA Emergency Use Authorization.

    Product
    AntIbody to SARS-CoV-2 - Product Usage: (Colloidal Gold) for IgG/IgM Diagnostic Kit, RAPID TEST DEVICE, Whole Blood/Serum/Plasma, SKY Medical Supplies and Equipments, LLC.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V104000·2021-02-23

    Bentley Recalls One 2020 Flying Spur for Fuel Tank Welding Defect

    Bentley is recalling one 2020 Flying Spur because the fuel tank may not have been welded properly, creating a risk of fuel leak and fire.

    Product
    BENTLEY — BENTLEY FLYING SPUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V106000·2021-02-23

    Mercedes-Benz Metris Recall for Improperly Welded Front Passenger Seat Frame

    Daimler Vans USA is recalling 2021 Mercedes-Benz Metris vans because the front passenger seat frame base may not have been welded properly, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V101000·2021-02-22

    2021 Mazda Mazda3 and CX-30 tire air valve failure recall

    Mazda is recalling 2021 Mazda3 and CX-30 vehicles because air may leak from the tire air valve, potentially causing loss of vehicle control. Mazda will replace all tire air valves at no cost.

    Product
    MAZDA — MAZDA MAZDA3, CX-30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V102000·2021-02-22

    Mercedes-Benz Recalls 2021 GLA 250 for Air Bag Ground Connection Defect

    Mercedes-Benz is recalling 2021 GLA 250 vehicles because the front passenger air bag ground connection may be improperly mounted, risking inadvertent deployment.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V100000·2021-02-19

    KME Recalls TDA Firetrucks Due to Trailer Brake Wiring Defect

    KME is recalling 2001-2020 TDA tractor-drawn aerial firetrucks because incorrect wiring in the trailer's ABS control module may cause brake failure, increasing crash risk.

    Product
    KME — KME TDA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·005-2021·2021-02-19

    USDA Recalls Pork Pâté Imported Without Inspection

    AH Company International Distribution is recalling approximately 30,081 pounds of Monique Ranou pork pâté products imported without FSIS re-inspection.

    Product
    AH Company International Distribution, Inc., Recalls Pork Products Imported Without the Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21T002000·2021-02-19

    Cooper Tire Recalls Multiple Tires Due to Sidewall Separation Risk

    Cooper Tire is recalling specific Discoverer, Evolution, and other brand tires because the sidewall may bulge or separate, potentially causing a rapid deflation and crash.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V097000·2021-02-19

    KME Predator Fire Trucks Recalled for Insufficient Rear Axle Welds

    KME is recalling certain Predator fire trucks because rear axle welds may be insufficient, potentially causing loss of vehicle control and increasing crash risk.

    Product
    KME — KME PREDATOR PUMPER, PREDATOR RESCUE, PREDATOR PANTHER PUMPER, PREDATOR SS PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V096000·2021-02-19

    BMW Recalls Multiple 2019-2021 Models for Rearview Camera Software Issues

    BMW is recalling 13,858 vehicles from 2019-2021 model years due to rearview camera software issues that may obscure visibility when reversing. Dealers will update the software free of charge.

    Product
    BMW — BMW M850I, 540I, 330E, 740I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V098000·2021-02-19

    2022 Volvo VNL trucks recalled for wheels that may bend or break

    Volvo Trucks is recalling certain 2022 VNL trucks with Alcoa Mirror Polish Wheels that may fail to support the load, increasing crash risk. Affected wheels will be replaced at no cost by dealers.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V092000·2021-02-18

    Trail King Recalls 2021 TKSA Trailers Due to Frame Crack Risk

    Trail King is recalling 2021 TKSA trailers because a cross member in the slide pan frame may crack and detach, increasing crash risk.

    Product
    TRAIL KING — TRAIL KING TKSA
    Category
    Vehicle
    Distribution
    Distributed nationwide