The Recall Desk

State

New Hampshire product recalls

73,833 recalls have nationwide distribution and so reach New Hampshire. 4,483 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total
4,483
Critical
603
Severe
1,049
Most recent
2026-11-04

Of the 4,483 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 1,049 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,483 recalls whose distribution notice names New Hampshire specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50776–50800 of 78316

  • ModerateFDA (Devices)·Z-2004-2016·2016-07-13

    Musculoskeletal Transplant Foundation Recalls AFT Diverted Tubes Due to Unsealed Pouch

    Musculoskeletal Transplant Foundation is recalling 114 AFT Diverted Tubes because an unsealed Tyvek pouch could introduce contamination into the sterile field.

    Product
    Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of surgically-created osseous defects or osseous defects created from traumatic injury. It can be used in the: extremities, pelvis, and spine. Product Code: 227005.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1065-2016·2016-07-13

    Allergan Recalls Tazorac Gel 0.05% Sample Packs for Content Uniformity Failure

    Allergan Sales, LLC is recalling Tazorac (tazarotene) Gel 0.05% sample packs due to failed content uniformity specifications.

    Product
    Tazorac (tazarotene) Gel 0.05%, 15 x 3.5g, sample packs, Allergan Inc, Irvine, CA 92612. UPC 300238335159
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1064-2016·2016-07-13

    Allergan Recalls Tazorac Gel 0.05% Due to Content Uniformity Failures

    Allergan is recalling Tazorac (tazarotene) Gel 0.05% because the product failed content uniformity specifications. The recall covers 17,802 units distributed nationwide and in Puerto Rico.

    Product
    Tazorac (tazarotene) Gel 0.05%, Rx only, packaged in a) 30g (NDC 0023-8335-03) and b) 100g (NDC 0023-8335-10) tubes, Allergan Inc, Irvine, CA 92612
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2120-2016·2016-07-13

    ZYTO Technologies Recalls ZYTO Tower and Software for Regulatory Violations

    ZYTO Technologies is voluntarily recalling ZYTO Tower devices and software because their marketing claims exceeded the scope of their FDA 510(k) clearance.

    Product
    The ZYTO Tower is the input device to program the software with various virtual items.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1618-2016·2016-07-13

    Zarbee's Recalls Baby Vitamin D Liquid Due to Contaminants

    Zarbee's Naturals is recalling specific lots of Baby Vitamin D liquid supplements because some units contain elevated aerobic plate counts and do not meet visual appearance standards.

    Product
    Baby Vitamin D Dietary supplement (in liquid form), 15 ml and 14 ml in glass bottle with dropper dispenser.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2138-2016·2016-07-13

    Synthes Ti Button Plate Recalled for Inaccurate MR Safety Labeling

    Synthes (USA) Products LLC is recalling 6,255 Ti Button Plate units because their MR safety information does not meet current ASTM standards.

    Product
    Synthes Ti Button Plate 7 Holes, Fastener, Fixation, nondegradable, Soft Tissue
    Category
    Medical Device
    Distribution
    50 states
  • ModerateFDA (Devices)·Z-2083-2016·2016-07-13

    Medtronic Navigation O-arm 02 surgical x-ray system recalled for labeling gaps

    Medtronic Navigation is recalling 63 O-arm 02 surgical x-ray imaging systems nationwide due to gaps in electronic product labeling and Instructions for Use compliance.

    Product
    Medtronic Navigation O-arm 02 surgical x-ray imaging system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2121-2016·2016-07-13

    ZYTO Software Recalled for Exceeding 510(k) Clearance Claims

    ZYTO Technologies is voluntarily recalling ZYTO Tower and software programs because their claims exceeded the scope of their FDA 510(k) clearance.

    Product
    The ZYTO Select and ZYTO Elite software programs are used to rank pairs of galvanic skin response measurements from most coherent (the second scan is closest in time measurement to the baseline original scan) to least coherent (further away from the baseline).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2128-2016·2016-07-13

    Exactech Recalls Novation Hip Stems Due to Incorrect GTIN Labeling

    Exactech is recalling 14 Novation femoral stems because they were labeled with an incorrect Global Trade Item Number (GTIN). The error identifies the devices as a different product.

    Product
    Novation Press-Fit Splined RDD, Extended Offset, HA Coated, 12/14 Taper Femoral Stems, Size 18. Femoral stems are indicated for use in skeletally mature individuals undergoing primary surgery for hip replacement due to osteoarthritis, rheumatoid arthritis, osteonecrosis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2119-2016·2016-07-13

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Products Calibrator Kit 29

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 29 because incorrect calibration mathematics may cause biased test results for total iron-binding capacity.

    Product
    VITROS Chemistry Products Calibrator Kit 29, REF/Product Code 680 2344, used in conjunction with VITROS Chemistry Products dTIBC Reagent Generation 30 (GEN 30), REF 680 2001, and Assay Data Disk (ADD), REF/Product Code 6801876 (Unique Device No. 10758750001576), Data Release…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2127-2016·2016-07-13

    Exactech Recalls Hip Replacement Stems Due to Incorrect GTIN Labeling

    Exactech is recalling 8 units of Novation Press-Fit Splined Femoral Stems because they are labeled with an incorrect Global Trade Item Number (GTIN).

    Product
    Novation Press-Fit Splined RDD, Extended Offset, HA Coated, 12/14 Taper Femoral Stems, Size 17. Product Usage Femoral stems are indicated for use in skeletally mature individuals undergoing primary surgery for hip replacement due to osteoarthritis, rheumatoid arthritis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V529000·2016-07-12

    Chrysler Recalls Vehicles for Transmission Wire Harness Defect

    Chrysler is recalling specific 2014-2016 vehicles because a transmission wire harness defect may cause the vehicle to unexpectedly shift to neutral, increasing crash risk.

    Product
    FIAT — FIAT, CHRYSLER, RAM 500X, 200, PROMASTER, CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V527000·2016-07-12

    Nissan Recalls 2012-2013 Infiniti M35 Hybrid for Engine Shutdown Risk

    Nissan is recalling 1,140 Infiniti M35 Hybrid vehicles because a system overheat may cause the engine to shut off while driving, increasing crash risk.

    Product
    INFINITI — INFINITI M35 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·058-2016·2016-07-12

    Simmons Recalls Frozen Chicken Fritters Due To Possible E. Coli O121

    Simmons Prepared Foods is recalling approximately 5,850 pounds of frozen, heat-treated chicken fritters due to possible E. coli O121 contamination from recalled flour.

    Product
    Simmons Prepared Foods, Inc. — Simmons Prepared Foods, Inc. Recalls Chicken Products Due To Possible E. Coli O121 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V525000·2016-07-11

    Heil Recalls 2014-2016 Trailers Due to Spring Brake Valve Defect

    Heil is recalling 2014-2016 trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.

    Product
    HEIL — HEIL FLATBED, PETROLEUM PULL TRAILER, DRY BULK TRAILER, CRUDE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V524000·2016-07-11

    Polar Tank Trailer Recalls 2014-2016 Models Due to Brake Delay

    Polar Tank Trailer is recalling 2014-2016 tank trailers because improperly machined brake valves may delay spring brake application, increasing the risk of the trailer rolling away.

    Product
    POLAR TANK — POLAR TANK MC 331 TANK TRAILER, DOT 412 TANK TRAILER, DOT 406 TANK TRAILER, NON-CODE TANK TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E061000·2016-07-11

    Can-Am Spyder F3-T Recall for Passenger Seat Stability Issue

    Bombardier is recalling Can-Am Spyder F3-T motorcycles because an accessory passenger seat may fail to activate the vehicle stability system, increasing crash risk.

    Product
    CAN-AM — CAN-AM SPYDER F3-T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V526000·2016-07-11

    Honda Recalls 2016 Civic 2-Door Vehicles for Taillight Defect

    Honda is recalling 2016 Civic 2-Door vehicles because a damaged circuit board may cause side marker lights to fail, reducing visibility.

    Product
    HONDA — HONDA CIVIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V523000·2016-07-11

    MANAC Recalls 2016-2018 Trailers Due to Spring Brake Valve Defect

    MANAC is recalling 2016 Flatbed and 2017-2018 Van trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.

    Product
    MANAC — MANAC VAN TRAILER, FLATBED
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·057-2016·2016-07-08

    Kabob's Acquisition Recalls Raw Meat and Poultry Due to E. Coli O121

    Kabob's Acquisition, Inc. is recalling approximately 44,850 pounds of raw meat and poultry products due to possible E. coli O121 contamination.

    Product
    Kabobs Aquisition, LLC — Kabob's Acquisition, Inc. Recalls Not Ready-To-Eat Meat and Poultry Products Due to Possible E. Coli O121 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V519000·2016-07-08

    Audi Recalls 2017 Q7 Models Due to Air Bag Software Defect

    Volkswagen is recalling 2017 Audi Q7 vehicles because a software issue may cause frontal air bags to deploy with excessive force, increasing injury risk.

    Product
    AUDI — AUDI Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide