The Recall Desk

State

New Hampshire product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42901–42925 of 78300

  • HighFDA (Devices)·Z-0174-2018·2017-12-06

    Siemens Dimension Vista Protein 1 Control Recalled for Inaccurate Ceruloplasmin Assignment

    Siemens Healthcare Diagnostics is recalling Dimension Vista Protein 1 Control lots due to inaccurate ceruloplasmin assignment, which may cause patient results to fall below the reference range.

    Product
    Dimension Vista Protein 1 Control, PROT 1 CON L, Siemens Material Number (SMN) 10445919, Product Code KC715; IVD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0189-2018·2017-12-06

    Volcano Imaging Systems Recalled Due to Unexpected Windows Security Dialog

    Volcano Corporation is recalling specific intravascular ultrasound imaging systems because an unexpected Microsoft Windows Security dialog may appear during use, potentially affecting device operation.

    Product
    Volcano Imaging System s5i REF 807400001; CORE Mobile Imaging System (120V) REF 400-0100.01; CORE Mobile Imaging System Refurbished REF 400-0100.01-R; CORE Mobile Imaging System (240V) REF 400-0100.07; CORE Mobile Imaging System Refurbished REF 400-0100.07-R; CORE Mobile Imaging…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0184-2018·2017-12-06

    Zimmer Biomet Recalls ROSA Surgical Device Due to Software Issue

    Zimmer Biomet is recalling 29 ROSA Surgical Devices due to a software issue in the MXTTOUT controller parameter settings.

    Product
    ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled electromechanical arm. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0181-2018·2017-12-06

    Arrow PICC Kits Recalled for Potential Incorrect Sheath Size

    Arrow International is recalling specific PICC kits that may contain 5 Fr peel-away sheaths instead of the required 4 Fr size.

    Product
    ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable PICC is indicated for short or long term peripheral access to the central venous system for intravenous therapy, blood sampling, infusion, power injection of contrast media and allows for central venous pressure…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0183-2018·2017-12-06

    BD Insulin Syringes Recalled for Incorrect Needle Length Labeling

    Becton Dickinson is recalling specific lots of BD Insulin Syringes because some polybags were mislabeled with the wrong needle length and gauge.

    Product
    BD Insulin Syringes with the BD Ultra-Fine(TM) needle ¿ mL 12.7mm 30G, Catalog/REF 328466 BD Insulin Syringes are intended for the subcutaneous injection of insulin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0173-2018·2017-12-06

    Siemens Dimension Vista Protein 1 Calibrator Recalled for Inaccurate Ceruloplasmin Results

    Siemens is recalling Dimension Vista Protein 1 Calibrators because they may produce inaccurate ceruloplasmin results below the reference range.

    Product
    Dimension Vista Protein 1 Calibrator, PROT 1 CAL, Siemens Material Number (SMN) 10465664 (US) and 10469516 (OUS), Product Code KC710U (US) and KC710 (OUS); IVD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0182-2018·2017-12-06

    Arrow International Recalls Pressure Injectable PICC Kits Due to Sheath Error

    Arrow International Inc. is recalling specific lots of ADVANTAGE 5" Pressure Injectable PICC kits because they may contain 5 Fr peel-away sheaths instead of the required 4 Fr sheaths.

    Product
    ArrowADVANTAGE5" Pressure Injectable Peripherally Inserted Central Catheter (PICC) The Pressure Injectable PICC is indicated for short or long term peripheral access to the central venous system for intravenous therapy, blood sampling, infusion, power injection of contrast…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0096-2018·2017-12-06

    Teva Recalls Clozapine Tablets Due to Potential Broken Tablets

    Teva Pharmaceuticals USA is recalling 3,870 bottles of Clozapine Tablets USP, 100 mg, due to failed specifications and potential broken tablets.

    Product
    Clozapine Tablets USP, 100 mg, 500 count bottles, Rx only, Manufactured in Israel by: TEVA PHARMACEUTICALS IND, LTD, Jerusalem Israel, Manufactured For: TEVA PHARMACEUTICALS USA, North Wales, PA, NDC 00093-7772-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0100-2018·2017-12-06

    Vertra Sunscreen Recalled for Manufacturing Quality Deviations

    EAI-JR286 Inc. is recalling 5,355 tubes of Vertra Elemental Resistance Sunscreen due to manufacturing deviations that may impact product quality.

    Product
    Vertra Elemental Resistance (Octyl Methoxycinnamate 6%, Oxybenzone 5%, Titanium Dioxide 6.3%, Zinc Oxide 9.9%) Sun Protection Cream, SPF 50+, Net. Wt. 2.8 oz (80 g) tube in a carton, Distributed by Vertra/EAI-JR286, 20100 S Vermont Ave, Torrance, CA 90502, Made In Australia, UPC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0179-2018·2017-12-06

    Arrow VPS Access Kit Recalled for Potential Size Mismatch

    Arrow International is recalling VPS Access Kits because they may contain 5 Fr peel-away sheaths instead of the required 4 Fr size.

    Product
    Arrow(R) VPS(R) Access Kit for use with 4 Fr. Peripherally Inserted Central Venous Catheter The intended use of the VPS Stylet and Console (VPS System) is to quickly and accurately guide market available peripherally inserted central catheters (PICCs) to the goal location which…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0185-2018·2017-12-06

    Implant Direct Legacy Dental Implants Recalled for Packaging Defect

    Implant Direct Sybron Manufacturing is recalling 75 units of Legacy 3 Dental Implants because a packaging defect may compromise sterilization.

    Product
    ImplantDirect Legacy(TM) 3 Implant, 13MM L, REF 864713 This Legacy implant is a two-piece implant for one-stage or two-stage surgical procedures. These implants are intended for use in partially and fully edentulous upper and lower jaws in support of single or multiple-unit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0180-2018·2017-12-06

    Arrow PICC Recall Due to Potential Incorrect Peel-Away Sheath Size

    Arrow International is recalling specific lots of ARROW PICC powered by ARROW VPS Stylet kits that may contain 5 Fr peel-away sheaths instead of the required 4 Fr.

    Product
    ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable PICC is indicated for short or long term peripheral access to the central venous system for intravenous therapy, blood sampling, infusion, power injection of contrast media and allows for central venous pressure…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0098-2018·2017-12-06

    Mayne Pharma Recalls Liothyronine Sodium Tablets for Dissolution Failures

    Mayne Pharma Inc is recalling 11,364 bottles of Liothyronine Sodium Tablets 25 mcg because they failed dissolution specifications. The affected lot is distributed nationwide.

    Product
    Liothyronine Sodium Tablets, USP 25 mcg ,100-count bottles, Rx Only, Distributed by Perrigo Minneapolis, MN 55427, NDC 0574-0222-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0188-2018·2017-12-06

    Medtronic Recalls Everflex Self-Expanding Peripheral Stents Due to Labeling Error

    Medtronic is recalling 21 units of Everflex Self-Expanding Peripheral Stents because the stent length on the label may not match the actual stent length.

    Product
    Everflex Self-Expanding Peripheral Stent with Entrust Delivery System Intended to improve luminal diameter in the treatment of symptomatic de-novo or restenotic lesions up to 140 mm in length in the native Superficial Femoral Artery (SFA) and/or proximal popliteal arteries…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0397-2018·2017-12-06

    Pure Encapsulations AI Enzymes Recalled for Undeclared Sulfites

    Pure Encapsulations is recalling AI Enzymes dietary supplements because they contain undeclared sulfites. The products were distributed in five states.

    Product
    pure encapsulations AI Enzymes DIETARY SUPPLEMENT 120 CAPSULES UPC: 7 66298 00318 4 and 60 CAPSULES UPC: 7 66298 00317 7
    Category
    Food
    Distribution
    5 states
  • SevereCPSC·18047·2017-12-05

    Netgear Recalls Outdoor Camera Power Adapters Due to Fire Hazard

    Netgear is recalling VMA4700 power adapters for Arlo outdoor cameras because water leakage can cause short circuits, melting, and fire.

    Product
    Power adapters for outdoor Arlo cameras
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18053·2017-12-05

    Metabo Recalls Rat Tail Angle Grinders Due to Laceration Hazard

    Metabo is recalling specific rat tail angle grinders because the on-off switch can lock in the on position, posing a laceration hazard.

    Product
    Rat tail angle grinders with brake
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V776000·2017-12-04

    Burch Recalls 1984 Evans Cargo Tank Trailers Due to Brake Caliper Bolts

    Burch Tank and Truck is recalling 1984 Evans Cargo Tank trailers because improperly torqued brake caliper bolts may allow the caliper to detach, increasing crash risk.

    Product
    EVANS — EVANS CARGO TANK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V778000·2017-12-04

    Triple E RV Recalls 2016-2018 Wonder Motorhomes for Seat Bolt Issue

    Triple E RV is recalling 2016-2018 Wonder motorhomes because improperly tightened passenger seat bolts may fail in a crash, increasing injury risk.

    Product
    TRIPLE E RV — TRIPLE E RV WONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V777000·2017-12-04

    Temsa Recalls 2017-2018 Buses Due to Fire Suppression Chemical Contamination

    Temsa is recalling 2017-2018 TS30, TS35E, and TS45 buses because the fire suppression system may contain contaminated dry chemical, which could discharge improperly and increase injury risk.

    Product
    TEMSA — TEMSA TS45, TS30, TS35E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V775000·2017-12-01

    Ford Recalls 2018 Expedition Vehicles for Seat Back Bolt Defect

    Ford is recalling 2018 Expedition vehicles because second-row outboard seats may have improperly installed bolts or excessive forward adjustment, increasing injury risk in a crash.

    Product
    FORD — FORD EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V772000·2017-12-01

    MV Agusta Recalls 2017 Brutale 800 Dragster RR for Rear Wheel Spokes

    MV Agusta is recalling 45 2017 Brutale 800 Dragster RR motorcycles because rear wheel spokes may loosen, potentially affecting handling and increasing crash risk.

    Product
    MV AGUSTA — MV AGUSTA BRUTALE 800 DRAGSTER RR
    Category
    Vehicle
    Distribution
    Distributed nationwide