State

New Hampshire product recalls

73,741 recalls have nationwide distribution and so reach New Hampshire. 4,482 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total: 4,482
Critical: 603
Severe: 1,048
Most recent: 2026-10-28

Of the 4,482 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 4,482 recalls whose distribution notice names New Hampshire specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36076–36100 of 78223

LowFDA (Devices)·Z-1080-2019·2019-04-10
McKesson Consult Diagnostic Fecal Occult Blood Test Recalled for Packaging Issues
Cypress Medical Products LLC is recalling McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Tests because the packaging is too similar to other products, leading to a denial of CLIA waiver approval.
Product
McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test, Part numbers 178-CK30T, 178-CT30, 178¿TBSO, 178-CM25, 178-CK50, 178-CM50, 178-CT50, 178¿CK30
Category
Medical Device
Distribution
27 states
LowFDA (Drugs)·D-1067-2019·2019-04-10
Pfizer Recalls Cleocin Phosphate Injection Due to Impurity Failures
Pfizer is recalling specific lots of Cleocin Phosphate injection because high out-of-specification impurities were detected at the 24-month time point.
Product
CLEOCIN PHOSPHATE — CLEOCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19V283000·2019-04-09
Proterra Recalls 2015-2018 Catalyst Buses Due to Brake Fire Risk
Proterra is recalling 2015-2018 Catalyst 40 buses because a clogged tow fitting cap can cause rear brakes to overheat and catch fire.
Product
PROTERRA — PROTERRA CATALYST
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V282000·2019-04-09
Peterbilt 520 Recall: Undersized Wires May Cause Engine Shutdown
PACCAR is recalling 2017-2020 Peterbilt 520 trucks because undersized wires may overheat and melt, potentially causing an unexpected engine shutdown and increasing crash risk.
Product
PETERBILT — PETERBILT 520
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V281000·2019-04-09
Horton Ambulances Recalled for Reversed Backup Camera Image
Halcore Group is recalling 2016-2019 Horton ambulances because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.
Product
HORTON — HORTON TYPE I, TYPE III
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V284000·2019-04-09
Daimler Recalls 2019 Sprinter Vans for Headlight Sensor Calibration Issues
Daimler Vans USA is recalling 2019 Freightliner and Mercedes-Benz Sprinter vans because the headlamp range adjustment sensor may not be calibrated, potentially affecting driver visibility.
Product
FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V276000·2019-04-09
AEV TraumaHawk Ambulances Recalled for Reversed Backup Camera Image
Halcore Group is recalling 2016-2019 AEV TraumaHawk ambulances because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.
Product
AEV — AEV TRAUMAHAWK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V280000·2019-04-09
Pierce Frontline Vehicles Recalled for Brake Light Wiring Defect
Pierce is recalling 2018-2019 Frontline C-35X, C-25, C-45X-3, and Encore Rescue vehicles because brake lights may illuminate without the pedal being pressed.
Product
FRONTLINE — FRONTLINE C-25, C-35X, ENCORE RESCUE, C-45X-3
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·19102·2019-04-09
Marpac Recalls GO Travel Sleep Sound Machines Due to Burn Hazard
Marpac is recalling GO travel sleep sound machines because the internal battery can leak and cause an electrical short, posing a burn hazard.
Product
GO travel sleep sound machines
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·19V279000·2019-04-08
Load Trail Recalls 2018-2019 Dump Trailers Due to Bolt Failure Risk
Load Trail is recalling 2018-2019 dump trailers because bolts on the hydraulic cylinder can break under heavy loads, causing the dump box to lower rapidly.
Product
LOAD TRAIL — LOAD TRAIL TANDEM AXLE DUMP, TRIPLE AXLE DUMP
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V277000·2019-04-08
Audi Recalls 2018-2019 Q5 and SQ5 for Brake Master Cylinder Defect
Audi is recalling 2018-2019 Q5 and SQ5 vehicles because a short brake master cylinder casting could cause sudden brake loss, increasing crash risk.
Product
AUDI — AUDI Q5, SQ5
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V278000·2019-04-08
Ford Recalls F-Series Trucks Due to Block Heater Fire Risk
Ford is recalling 2015-2019 F-150 and 2017-2019 Super Duty trucks because a damaged block heater cable could cause a fire.
Product
FORD — FORD F-550 SD, F-350 SD, F-150, F-250 SD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V274000·2019-04-05
Nova Bus Recalls 2011-2019 LFS City Buses for Fire Risk
Nova Bus is recalling 2011-2019 LFS city buses because an engine door fan electrical connector may overheat and cause a fire.
Product
NOVA BUS — NOVA BUS LFS
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·042-2019·2019-04-05
J&J Snack Foods Recalls Stuffed Sandwiches Due to Plastic Contamination
J&J Snack Foods Handhelds Corp. is recalling Bremer hot stuffed sandwiches due to possible semi-transparent plastic contamination. No illnesses have been reported.
Product
J&J Snack Foods Handhelds Corp. — J&J Snack Foods Handhelds Corp. Recalls Stuffed Sandwich Products due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
HighNHTSA·19V275000·2019-04-05
Kenworth T680 and T880 Recalled for Parking Brake Signal Delay
PACCAR is recalling 2018-2020 Kenworth T680 and T880 trucks because a parking brake signal delay in cold weather may cause unexpected vehicle movement.
Product
KENWORTH — KENWORTH T680, T880
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V273000·2019-04-04
BMW Recalls 2006 Models Due to PCV Valve Fire Risk
BMW is recalling 2006 3, 5, and Z4 series vehicles because a heater in the PCV valve may short circuit, increasing the risk of a fire.
Product
BMW — BMW Z4, 530XI, 525I, 325XI
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·041-2019·2019-04-04
Blount Fine Foods Recalls Chicken Soup for Undeclared Milk Allergen
Blount Fine Foods is recalling frozen chicken soup products due to misbranding and an undeclared milk allergen. No adverse reactions have been reported.
Product
Blount Fine Foods — Blount Fine Foods Recalls Ready-To-Eat Chicken Soup Product due to Misbranding and an Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
HighCPSC·19099·2019-04-04
Vivitar Recalls Hot/Cold Massage Balls Due to Burn Hazard
Vivitar is recalling hot/cold massage balls sold at Target because they can leak or rupture during microwaving, posing a burn hazard.
Product
Hot/cold massage balls
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·19V272000·2019-04-04
Mazda Recalls 2016-2018 Mazda3 Vehicles for Windshield Wiper Relay Defect
Mazda is recalling 2016-2018 Mazda3 vehicles because a defective wiper relay may cause the wipers to stop working, reducing visibility and increasing crash risk.
Product
MAZDA — MAZDA MAZDA3
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1085-2019·2019-04-03
Blue Fusion Capsules Recalled for Undeclared Prescription Ingredients
Ata International Inc is recalling Blue Fusion Capsules because FDA analysis found undeclared prescription ingredients, including Sildenafil and Tadalafil.
Product
Blue Fusion Capsules, 1- count blister pack, Distributed by: DNS Distribution 5225 Canyon Crest Dr. Ste 71-640, Riverside, CA 92507, UPC 7 48252 66460 0
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1185-2019·2019-04-03
Utz Recalls Bachman Pretzels Due to Undeclared Milk Allergen
Utz Quality Food is recalling Bachman Original Twist Pretzels because butter pretzels were mistakenly packaged in regular pretzel bags, creating an undeclared milk allergen hazard.
Product
Bachman Original Twist Pretzels,10 oz.Bag (flexible film) UPC: 0-77817-10580-8
Category
Food
Distribution
12 states
SevereFDA (Devices)·Z-0986-2019·2019-04-03
Maquet Cardiohelp Emergency Drive Recalled for Gearwheel Assembly Defect
Maquet Cardiovascular is recalling 10 units of the Cardiohelp Emergency Drive because the gearwheel may have been incorrectly reassembled, leading to inadequate operation.
Product
Cardiohelp Emergency Drive, Part No. 70104.8002 Product Usage: The Cardiohelp Emergency Drive is used in emergencies to manually drive the disposable if the Cardiohelp-i fails.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1053-2019·2019-04-03
Philips UroDiagnost MRF Recall Due to Missing Locking Plate
Philips is recalling UroDiagnost MRF units because a missing locking plate may cause unexpected stand or table tilt movement that users cannot stop.
Product
Urodiagnost, Product No. 708033 Product Usage: The Philips UroDiagnost MRF can be used to perform all urological and gynecological routine examinations including: Urograms with injection or infusion Retrograde pyelography Cystography and urethrography Micturition…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1054-2019·2019-04-03
Philips OmniDiagnost X-ray System Recalled for Missing Locking Plate
Philips North America is recalling 1,696 OmniDiagnost Classic X-ray systems because a missing locking plate may cause unexpected stand or table movement that users cannot stop.
Product
Omnidiagnost Classic, Product Codes 70859, 708023, 708024, 708025 Product Usage: The Philips OmniDiagnost is a multi-functional, universal X-ray system with remote-controlled facilities. It performs a wide range of routine examinations and interventional procedures include…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V269000·2019-04-03
Weis Fire & Safety Recalls One 2018 Ford F-550 Emergency Vehicle
Weis Fire & Safety is recalling one 2018 Ford F-550 emergency vehicle because its brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.
Product
FORD — FORD F-550
Category
Vehicle
Distribution
Distributed nationwide