State

New Hampshire product recalls

73,584 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: 603
Severe: 1,048
Most recent: 2026-10-21

Of the 4,477 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 1,048 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,477 recalls whose distribution notice names New Hampshire specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

801–825 of 78061

ModerateFDA (Drugs)·D-0826-2026·2026-09-09
Allies Group Recalls Subpotent SPF 50 Sunscreen Gel
Allies Group Inc. is recalling 2,149 tubes of SPF 50 sunscreen gel because testing showed it may not provide the labeled sun protection.
Product
THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 90ml - 3 fl. oz. Tube, Made in the U.S.A, Distributed by Allies Group Pte Ltd, Singapore 068914. UPC 8 885014 075853
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3047-2026·2026-09-09
Diagnostica Stago Recalls STA Staclot Protein S Reagent Due to QC Drift
Diagnostica Stago is recalling 5,220 units of STA Staclot Protein S reagent because quality control values drifted within the stated stability period.
Product
STA Staclot Protein S, Model/Catalog Number: 00746-Reagent Lot number 273074; qualitative and quantitative factor deficiency test
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3102-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes
Cardinal Health is recalling specific urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, ROBOTIC HYST , Catalog Number: PB41RHRM3; 2) KIT, ROBOTIC HYST , Catalog Number: PB41RHRM4; 3) KIT, C SECTION , Catalog Number: PLVMCS22G…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3099-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes
Cardinal Health is recalling 60 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT,MAXILLOFACIAL PRESBYTERIAN, Catalog Number: PWV2MF01D
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0812-2026·2026-09-09
Baxter Recalls Pantoprazole Sodium Infusion Bags Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Pantoprazole Sodium infusion bags due to Current Good Manufacturing Practice (CGMP) deviations.
Product
PANTOPRAZOLE SODIUM — PANTOPRAZOLE SODIUM (PANTOPRAZOLE SODIUM IN 0.9% SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0830-2026·2026-09-09
Mylan Recalls Mycophenolate Mofetil Injection Due to Dissolution Failures
Mylan Pharmaceuticals is recalling Mycophenolate Mofetil for injection because it failed to meet dissolution specifications.
Product
MYCOPHENOLATE MOFETIL — MYCOPHENOLATE MOFETIL (MYCOPHENOLATE MOFETIL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0839-2026·2026-09-09
Mylan Recalls Prasugrel Tablets for Failed Dissolution and Stability Testing
Mylan Pharmaceuticals is recalling 47,662 bottles of Prasugrel 10mg tablets because they failed dissolution specifications and 18-month stability testing.
Product
PRASUGREL — PRASUGREL (PRASUGREL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3094-2026·2026-09-09
Cardinal Health Recalls Presource Packs with Potential Lubricant Contamination
Cardinal Health is recalling Presource Packs containing CliniClean Pericare Wipes due to potential lubricant contamination that may cause localized skin effects.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT,GYN LAPAROSCOPY DH , Catalog Number: PBOCGLN17
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3101-2026·2026-09-09
Cardinal Health Recalls Presource Packs with Potentially Contaminated Wipes
Cardinal Health 200, LLC is recalling 1,398 Presource Packs containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, BLO ROBOTIC GYN , Catalog Number: PBCGRGB28; 2) KIT , GYN MAJOR BARNES JEWIS, Catalog Number: PBVMLP22G; 3) KIT, GYN OPERATIVE LAPAROSCOPY, Catalog Number: PBVM0722D…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0837-2026·2026-09-09
Sage Products Recalls Chlorhexidine Gluconate Cloth Due to Cross Contamination
Sage Products, LLC is recalling 165,536 packages of 2% Chlorhexidine Gluconate Cloth due to cross-contamination with other products.
Product
CHLORHEXIDINE GLUCONATE — CHLORHEXIDINE GLUCONATE (CHLORHEXIDINE GLUCONATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0833-2026·2026-09-09
Supernus Recalls Trokendi XR Topiramate Capsules for Dissolution Failure
Supernus Pharmaceuticals is recalling Trokendi XR (topiramate) extended-release capsules because they failed dissolution specifications. The recall covers 11,304 bottles distributed nationwide.
Product
Trokendi XR, (topiramate) extended-release capsules, 50 mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391 USA, Manufactured for: Supernus Pharmaceuticals, Inc., Rockville, MD 20850 USA, NDC 17772-102-30.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0840-2026·2026-09-09
Buprenorphine Sublingual Tablets Recalled for Labeling Mix-up
American Health Packaging is recalling 10,953 cartons of Buprenorphine Sublingual Tablets due to a label mix-up. The affected lot is distributed nationwide.
Product
BUPRENORPHINE — BUPRENORPHINE (BUPRENORPHINE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-3089-2026·2026-09-09
B Braun Recalls Discofix Stopcock Sets Due to Incorrect Expiration Date
B Braun Medical Inc is recalling specific lots of Discofix Four Way Stopcock Extension Sets because the carton shipper labels display an incorrect expiration date.
Product
Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V575000·2026-09-07
Can-Am Recalls Motorcycles Due to Instrument Cluster Freezing Risk
Bombardier Recreational Products is recalling specific Can-Am motorcycles because the touchscreen instrument cluster may freeze or go blank, hiding critical safety information.
Product
CAN-AM — CAN-AM SPYDER RT, SPYDER F3, PULSE, ORIGIN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V574000·2026-09-04
Kibbi Recalls 2026-2027 Renegade RVs Due to Fire Risk
Kibbi is recalling 2026-2027 Renegade recreational vehicles because a rooftop fan component may overheat and cause a fire.
Product
RENEGADE — RENEGADE CLASSIC
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·26733·2026-09-03
Loyoda Adult Portable Bed Rails Recalled for Entrapment and Asphyxiation Risks
Loyoda adult portable bed rails are being recalled because they violate safety standards, posing risks of entrapment, asphyxiation, falls, and lacerations.
Product
Loyoda Adult Portable Bed Rails
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26736·2026-09-03
Gizoon Six-Drawer Double Dressers Recalled for Tip-Over and Entrapment Hazards
Gizoon Direct is recalling six-drawer double dressers due to tip-over and entrapment risks that can cause serious injury or death to children.
Product
Gizoon Six-Drawer Double Dressers
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26746·2026-09-03
Mondraker Recalls Mountain Bicycles with ONOFF S9 Carbon Handlebars
Mondraker USA is recalling specific mountain bicycles equipped with ONOFF S9 Carbon MTB handlebars because they may crack or fracture, posing a risk of serious injury or death.
Product
Mondraker mountain bicycles equipped with ONOFF S9 Carbon MTB handlebars.
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·26V573000·2026-09-03
Nova Bus Recalls LFS Models Due to Coolant Sensor Defect
Nova Bus is recalling 2022-2024 LFS and LFS Artic buses because a faulty coolant sensor may cause unexpected engine shutdowns, increasing crash risk.
Product
NOVA BUS — NOVA BUS LFS, LFS ARTIC
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·26734·2026-09-03
Amana Through-The-Wall Air Conditioners Recalled Due to Fire Risk
Daikin Comfort Technologies is recalling Amana Through-The-Wall air conditioners and heat pumps because a shorted component can cause fire and serious injury.
Product
Amana Through the Wall (TTW) air conditioners or heat pumps
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26730·2026-09-03
Alanca 6-Drawer Dressers Recalled for Tip-Over and Entrapment Hazards
Nanjing Wu Hai Smart Home Appliance Store is recalling Alanca 6-Drawer Dressers due to risks of serious injury or death from tip-over and entrapment.
Product
Alanca 6-Drawer Dressers
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26731·2026-09-03
CPSC Recalls Cambridge Audio Yoyo (M) Bluetooth Speakers Due to Fire Hazard
Audio Partnership is recalling Cambridge Audio Yoyo (M) Bluetooth speakers because their lithium-ion batteries can overheat and cause fires. No injuries have been reported.
Product
Cambridge Audio Yoyo (M) Portable Bluetooth Speakers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·26E062000·2026-09-03
Nova Bus Recalls Casco Engine Coolant Level Sensors
Nova Bus is recalling Casco engine coolant level sensors that may send false signals, causing unexpected engine shutdowns and increasing crash risk.
Product
ENGINE AND ENGINE COOLING:COOLING SYSTEM recall
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·26735·2026-09-03
Branch Recalls Ergonomic Chairs Due to Backrest Detachment Fall Hazard
Branch is recalling about 16,000 ergonomic chairs because the backrests can detach, posing a fall hazard. No injuries have been reported.
Product
Ergonomic Chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26739·2026-09-03
Skip Hop Recalls Elmo Silicone Teethers Due to Choking Hazard
Skip Hop is recalling Baby Sesame Street Elmo Silicone Teethers because the black eyes can detach if frozen, posing a choking risk.
Product
Baby Sesame Street Elmo Silicone Teethers
Category
Consumer Product
Distribution
Distributed nationwide