State

New Hampshire product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39926–39950 of 78292

HighFDA (Devices)·Z-2467-2018·2018-07-25
GE Medical Systems Recalls T2100 Microflex Drive Treadmill Units
GE Medical Systems is recalling T2100 Microflex Drive Treadmills because unaddressed spare parts may cause uncontrolled walking belt motion during stress tests.
Product
T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended for medical purposes, such as to redevelop muscles or restore motion to joints or for use as an adjunct treatment for obesity. Specifically the T210…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2316-2018·2018-07-25
Wescam MX-10 Surveillance Laser System Recalled for Ocular Hazard
Wescam Inc is recalling 29 MX-10 surveillance laser systems because the ocular hazard distance is longer than specified, posing a risk of eye exposure.
Product
MX-10 surveillance laser system Product Usage: The expected usage of the product is to facilitate observation and surveillance missions from safe standoff ranges.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2437-2018·2018-07-25
Siemens Dimension Vista MULTI 1 SDIL Diluent Recall for Defective Septum
Siemens is recalling 197 units of Dimension Vista MULTI 1 SDIL diluent due to a potential defect in the vial cap septum that may cause inaccurate test results.
Product
Dimension Vista¿ MULTI 1 SDIL, KD693, SMN# 10469971
Category
Medical Device
Distribution
53 states
HighFDA (Food)·F-1651-2018·2018-07-25
TR Toppers Chopped Chocolate Pretzel Pieces Recalled for Peanut Contamination
T R Toppers, Inc. is recalling Chopped Chocolate Pretzel Pieces due to potential peanut contamination. Consumers should check for Lot 10481 and stop using the product.
Product
TR Toppers Brand Chopped Chocolate Pretzel Pieces. Item number B160-075 GTIN 0 06 51844 10599 6, 7.5 Lbs. (3 x 2.5 Lbs. Bags), Best Kept Between 34¿F and 40¿F <50% Relative Humidity
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2439-2018·2018-07-25
Opgen Recalls AdvanDx QuickFISH Slides Due to Diminished Performance
Opgen Inc is recalling AdvanDx QuickFISH Slides because they may show diminished performance before their expiration date.
Product
AdvanDx QuickFISH Slides, a component of the QuickFish BC Fixation Kit - BC, REF QFFIXBC1-25, Catalog Number: CS012 Control slides included as a component of the QFFIXBC1-25. The slides will provide non-fluorescent, wettable surface with dimensions appropriate for testing…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2480-2018·2018-07-25
Cardinal Health Recalls Presource PBDS Kits Due to Leaking Gatorade Pouches
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Product
Presource PBDS, Kit, Common Diabetes. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0920-2018·2018-07-25
Hain Celestial Recalls alba BOTANICA Sunscreen Due to Incorrect Formulation
The Hain Celestial Group is recalling alba BOTANICA sport mineral sunscreen because the wrong product formulation was placed in the packages.
Product
alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc oxide 9.0%), spf 45, 170 g (6 oz) tubes packaged in a) 4 tubes per case; b) 8 pack shipper display; Manufactured By: The Hain Celestial Group, Inc., Lake Success, NY 11042, UPC 7 24742 01102 4.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2496-2018·2018-07-25
Philips Ingenuity Digital PET/CT System Recall for Pallet Assembly Defect
Philips is recalling 32 Ingenuity Digital PET/CT Systems because a block connecting the patient pallet to the couch may be assembled incorrectly, potentially causing a misaligned screw.
Product
Ingenuity Digital PET/CT System, Model 882446 with the following UDI's: (01)00884838059559(21)900004 (01)00884838059559(21)900005 (01)00884838059559(21)900006 (01)00884838059559(21)900007 (01)00884838059559(21)900008 (01)00884838059559(21)900009…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2482-2018·2018-07-25
Cardinal Health Recalls Presource PBDS Kits Due to Leaking Gatorade Pouches
Cardinal Health is recalling Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Product
Presource PBDS, Kit, No Spiro. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as part of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2484-2018·2018-07-25
Stryker Recalls Reprocessed Harmonic Ace Shears Due to Error Code
Stryker is recalling 180 reprocessed Harmonic Ace shears because they may display an error code preventing use.
Product
Reprocessed HARMONIC Ace¿ +7, 5mm Diameter Shears with Advanced Hemostasis (HARH), Item Number HARH36 Product Usage: The Reprocessed HARMONIC ACE¿+7, 5 mm Diameter Shears with Advanced Hemostasis are indicated for soft tissue incisions when bleeding control and minimal…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2436-2018·2018-07-25
Siemens Dimension Vista CTNI Sample Diluent Recalled for Defective Cap Septum
Siemens Healthcare Diagnostics is recalling 1,446 units of Dimension Vista CTNI Sample Diluent because a defective cap septum may cause erroneously elevated test results.
Product
Dimension Vista¿ CTNI Sample Diluent, KD692, SMN# 10445205
Category
Medical Device
Distribution
53 states
ModerateFDA (Devices)·Z-2430-2018·2018-07-25
Valeris Medical Recalls Apollo XT Suture Anchors Due to Material Mislabeling
Valeris Medical is recalling 113 Apollo XT Suture Anchors because the labels incorrectly identified the material as titanium instead of PEEK.
Product
Apollo XT Suture Anchor, 5.5 x 15 Product Usage: Apollo XT Suture Anchors are intended for: Shoulder - Rotator Cuff Repair - Bankart Repair - SLAP Lesion Repair - Biceps Tenodesis - Acromio-Clavicular Separation Repair - Deltoid Repair - Capisular Shift or Capsulolabral…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2468-2018·2018-07-25
Fx Solutions Proton Beam Therapy Heads Recalled for Blister Breach
Fx Solutions is recalling specific proton beam therapy heads due to a breach in the external blister packaging.
Product
Fx SOLUTIONS CENTERED HEAD CoCr 50x19, REF 106-5019 Product Usage: Device is designed to produce and deliver proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2483-2018·2018-07-25
Cardinal Health Recalls Presource PBDS Kits Due to Leaking Gatorade Pouches
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Product
Presource PBDS, Kit, No Spiro Diabetes. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2469-2018·2018-07-25
Fx Solutions Offset Heads Recalled for Blister Breach
Fx Solutions is recalling specific lots of Humelock Offset Heads due to a breach in the external blister packaging.
Product
Fx SOLUTIONS OFFSET HEAD CoCr 50x20, REF 106-5000 Product Usage: Device is designed to produce and deliver proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2442-2018·2018-07-25
Health Harmony Mobile App Recalled for Data Synchronization Delays
Intel-GE Care Innovations LLC is recalling the Health Harmony Mobile application because patient data sometimes failed to sync with the backend database in a timely manner.
Product
Health Harmony Mobile application software Product Usage: Care Innovations Health Harmony Mobile is intended as a communication tool to display medical device data from third party devices for patients to view, and to collect assessment (question & answers) from…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2438-2018·2018-07-25
Siemens Dimension Vista MULTI 2 SDIL Diluent Recall for Defective Septum
Siemens is recalling 1,195 units of Dimension Vista MULTI 2 SDIL diluent because a defective septum may cause erroneously elevated test results.
Product
Dimension Vista¿ MULTI 2 SDIL, KD694, SMN# 10483586
Category
Medical Device
Distribution
53 states
ModerateFDA (Devices)·Z-2481-2018·2018-07-25
Cardinal Health Recalls Presource PBDS Kits Due to Gatorade Pouch Seal Defect
Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.
Product
Presource PBDS, Kit, Common. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as part of the…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·18E060000·2018-07-24
SynTec Recalls School Bus Seats Due to Mounting Foot Defect
SynTec is recalling S3B 45-inch Restraint School Bus Seats because the mounting foot may pull through the bolted joint at the bus floor, increasing injury risk in a crash.
Product
SEATS recall
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·18192·2018-07-24
JCPenney Recalls Okie Dokie Shorts Due to Choking Hazard
JCPenney is recalling Okie Dokie Denim Patches Shortie shorts because the patches can detach, posing a choking hazard to young children.
Product
Okie Dokie Denim Patches Shortie shorts
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·18190·2018-07-24
Ross Stores Recalls Bistro Chairs Due to Frame Breakage and Fall Hazard
Ross Stores is recalling Bronze Hammered bistro chairs because the frames can break, posing a fall hazard. Consumers should stop using the chairs and return them for a full refund.
Product
Bistro chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·18V488000·2018-07-23
Karma Revero Recalled for Non-Compliant Driver Side Rearview Mirror Glass
Karma Automotive is recalling 2018 Revero vehicles because the driver's side exterior rearview mirror may use convex glass instead of flat glass, failing federal safety standards.
Product
KARMA — KARMA REVERO
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18E058000·2018-07-20
Meritor Recalls Wheel Studs Due to Potential Heat Treatment Defect
Meritor is recalling specific wheel studs installed in steer axle hubs because improper heat treatment may cause them to fail, potentially leading to wheel detachment.
Product
WHEELS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18E059000·2018-07-20
Jost Recalls Fifth Wheel Assemblies Due to Narrow Bracket Risk
Jost International is recalling certain Outboard Sliders because a narrow bracket may allow the trailer to separate from the tractor, increasing crash risk.
Product
TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V489000·2018-07-20
BraunAbility Recalls Wheelchair Vans Due to Brake Line Connection Defect
Braun Corporation is recalling 2012-2018 BraunAbility Dodge and Chrysler wheelchair vans because brake lines may be disconnected, reducing electronic stability control performance.
Product
BRAUNABILITY — BRAUNABILITY DODGE WHEELCHAIR VAN, CHRYSLER WHEELCHAIR VAN
Category
Vehicle
Distribution
Distributed nationwide