State

New Hampshire product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47676–47700 of 78307

SevereFDA (Food)·F-0819-2017·2017-01-04
Cargill Recalls Wilbur Semi-Sweet Chocolate Drops for Undeclared Milk
Cargill Cocoa & Chocolate is recalling 50 lb. cartons of Wilbur Semi-Sweet Chocolate Drops because they may contain undeclared milk.
Product
Wilbur; IM10021; B558 Semisweet Chocolate Drops, 2000 CT; Net Weight 50 lb.; This item may contain dairy products; Cargill Cocoa & Chocolate, Inc., Lititz, PA 17543; BATCH 28116AANCB and 28116AANCC Material number: 100000081 packed in cardboard boxes.
Category
Food
Distribution
Distributed nationwide
HighCPSC·17063·2017-01-04
Disney Recalls Infant Hoodies Due to Choking Hazard from Detaching Snaps
Walt Disney Parks and Resorts is recalling Minnie and Mickey Mouse infant hoodie sweatshirts because the snaps can detach, posing a choking hazard to young children.
Product
Minnie and Mickey Mouse infant hoodie sweatshirts
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0907-2017·2017-01-04
GE Healthcare Recalls CRT Monitors Due to Potential Fall Hazard
GE Healthcare is recalling specific CRT monitors due to a risk that aged units may fall. The recall affects multiple imaging system models.
Product
ADVANTX LCN+
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-0904-2017·2017-01-04
GE Healthcare Recalls Innova 2000 Systems Due to Monitor Fall Risk
GE Healthcare is recalling Innova 2000 and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and abroad.
Product
Innova 2000
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-0914-2017·2017-01-04
GE Healthcare Recalls Prestilix Systems Due to Potential Monitor Fall Hazard
GE Healthcare is recalling Prestilix and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and overseas.
Product
Prestilix
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-0916-2017·2017-01-04
GE Healthcare Recalls X-Ray Systems Due to CRT Monitor Fall Risk
GE Healthcare is recalling specific X-ray systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.
Product
SFX
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-0908-2017·2017-01-04
GE Healthcare Recalls ADVANTX LCV+ Systems Due to CRT Monitor Fall Risk
GE Healthcare is recalling ADVANTX LCV+ systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.
Product
ADVANTX LCV+
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-0906-2017·2017-01-04
GE Healthcare Recalls CRT Monitors Due to Potential Fall Hazard
GE Healthcare is recalling specific CRT monitors due to the potential for the units to fall. The recall affects multiple system models including ADVANTX and Prestige.
Product
ADVANTX LCLP+
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-0901-2017·2017-01-04
Medtronic NIM EMG Endotracheal Tubes Recalled for Exposed Wire Hazard
Medtronic Xomed is recalling NIM EMG Endotracheal Tubes because wire in the tubing can become exposed, posing potential harm to intubated patients.
Product
NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually packaged.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0910-2017·2017-01-04
GE Healthcare Recalls Precision 500D Systems Due to Monitor Fall Risk
GE Healthcare is recalling Precision 500D and other systems because aged CRT monitors may fall.
Product
Precision 500D
Category
Medical Device
Distribution
41 states
HighCPSC·17064·2017-01-04
Toshiba Laptop Battery Packs Recalled for Overheating and Fire Hazards
Toshiba is expanding a recall of Panasonic lithium-ion battery packs for laptops due to overheating, burn, and fire risks. No injuries have been reported.
Product
Panasonic battery packs used in Toshiba laptop computers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0911-2017·2017-01-04
GE Healthcare Recalls Prestige II Systems Due to CRT Monitor Fall Risk
GE Healthcare is recalling Prestige II and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and abroad.
Product
Prestige II
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-0913-2017·2017-01-04
GE Healthcare Recalls Prestige VH and Other Systems Due to CRT Fall Risk
GE Healthcare is recalling Prestige VH and other medical systems because aged CRT monitors may fall.
Product
Prestige VH
Category
Medical Device
Distribution
41 states
HighCPSC·17722·2017-01-04
Curio Design Recalls Modular Light Kits and Bases for Shock and Fire Hazards
Curio Design is recalling Splyt modular light kits and bases because cracked pieces and faulty wires pose shock and fire hazards. No injuries have been reported.
Product
Modular light kits and bases
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0909-2017·2017-01-04
GE Healthcare Recalls Legacy Systems Due to CRT Monitor Fall Risk
GE Healthcare is recalling Legacy and other imaging systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.
Product
Legacy
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-0912-2017·2017-01-04
GE Healthcare Recalls Prestige SI Systems Due to CRT Monitor Fall Risk
GE Healthcare is recalling Prestige SI and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and overseas.
Product
Prestige SI
Category
Medical Device
Distribution
41 states
ModerateFDA (Food)·F-0906-2017·2017-01-04
Bio-Botanica Recalls Vitamin D-3 Drops for Excess Dosage
Bio-Botanica is recalling Nature's Answer and Seeking Health Vitamin D-3 drops because the lots contain more Vitamin D3 than the label claims.
Product
Liquid VITAMIN D-3 Drops distributed under the following private labels and sizes: a) NATURE'S ANSWER VITAMIN D-3 DROPS DIETARY SUPPLEMENT, 0.5 FLUID OZ/15 mL, UPC 8300026132 -- Nature's Answer Hauppauge, NY 11788; and b) Seeking Health Optimal Vitamin D, Liquid Vitamin D-3…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0240-2017·2017-01-04
Virtus Pharmaceuticals Recalls Virt-Select Prenatal Softgels Due to GMP Deviations
Virtus Pharmaceuticals is recalling Virt-Select Prenatal/Postnatal Softgels because the active ingredient manufacturer is on an FDA Import Alert for cGMP deviations.
Product
Virt-Select Prenatal/Postnatal Softgels, Prescription Multivitamin/Mineral Dietary Supplement with Fish-Based DHA , packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-249-30
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0903-2017·2017-01-04
Ortho-Clinical Diagnostics Recalls VITROS Intact PTH Reagent Packs
Ortho-Clinical Diagnostics is recalling VITROS Intact PTH Reagent Packs due to a positive bias of up to 20% and an incorrectly set reference interval.
Product
VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN 10758750006287 / Product Code 6802892 - Reagent Pack, 2) UPN 10758750006250 / Product Code 6802893 - Calibrators For the quantitative measurement of intact parathyroid hormone (iPTH) in human serum and plasma…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0241-2017·2017-01-04
VirtPrex Prenatal Tablets Recalled Due to API Manufacturer Import Alert
Virtus Pharmaceuticals is recalling VirtPrex Prenatal/Postnatal Tablets because the active ingredient manufacturer is on an FDA Import Alert.
Product
VirtPrex Prenatal/Postnatal Tablets, Prescription Supplement Containing Folic Acid and DHA, packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-348-30
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0235-2017·2017-01-04
Care-Tech Recalls Surgical Hand Scrub Due to Labeling and Cap Defects
Care-Tech Laboratories is recalling Techni-Care Surgical Hand Scrub because bottles have missing or illegible lot and expiration dates, as well as defective or cracked caps.
Product
Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation (3.0% w/v Chloroxylenol), packaged in a) 4 oz. bottles (NDC 46706-201-01), b) 8 oz bottles (NDC 46706-201-02), c) 16 oz. bottles (NDC 46706-201-03), d) 12 oz. pumpette (NDC 46706-201-05), e) 32 oz. bottles…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0239-2017·2017-01-04
Virtus Pharmaceuticals Recalls Extra-Virt Plus DHA Prenatal Softgels
Virtus Pharmaceuticals is recalling 2,406 bottles of Extra-Virt Plus DHA Prenatal/Postnatal Softgels because the API manufacturer is on FDA Import Alert.
Product
Extra-Virt Plus DHA Prenatal/Postnatal Softgel, Prescription Multivitamin/Mineral Dietary Supplement with Fish-Based DHA , packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-251-30
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0238-2017·2017-01-04
Virt-Advance Prenatal Softgels Recalled Due to API Manufacturer Import Alert
Virtus Pharmaceuticals is recalling Virt-Advance Prenatal/Postnatal Softgels because the active ingredient manufacturer is on an FDA Import Alert.
Product
Virt-Advance Prenatal/Postnatal Softgels, Prescription Folic Acid Containing Dietary Supplement, packaged in 90-count bottle, Rx only, Made in Canada, NDC 76439-357-90
Category
Drug
Distribution
Distributed nationwide
CriticalNHTSA·17E001000·2017-01-03
Takata Frontal Passenger Air Bag Inflator Rupture Recall
Takata is recalling certain frontal passenger air bag inflators that may rupture due to propellant degradation, posing a risk of serious injury or death.
Product
AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
CriticalNHTSA·17E002000·2017-01-03
Takata Frontal Passenger Air Bag Inflator Module Recall
Takata is recalling specific frontal passenger air bag inflators in 2012 vehicles registered in 14 states and territories due to a risk of rupture.
Product
AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide