State

New Hampshire product recalls

73,388 recalls have nationwide distribution and so reach New Hampshire. 4,472 additional recalls listed New Hampshire specifically in their distribution scope.

What the numbers show

Total: 4,472
Critical: 606
Severe: 1,042
Most recent: 2026-09-23

Of the 4,472 recalls naming New Hampshire we have scored against our rubric, 606 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,042 (23%) are Severe.

Which agencies issued them

These figures cover only the 4,472 recalls whose distribution notice names New Hampshire specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20701–20725 of 77860

SevereFDA (Food)·F-1362-2022·2022-07-06
Snack Sensations Apple, Pretzel & Celery Bites Recalled for Salmonella
Stellex/CF Houston, LLC is recalling Snack Sensations Apple, Pretzel & Celery Bites with Peanut Butter due to potential Salmonella contamination. The product was distributed across multiple states from May 2021 to June 2022.
Product
Snack Sensations Apple, Pretzel & Celery Bites with Peanut Butter Net Wt. 4 oz. packed in clear non-flexible plastic package UPC 0 74641 07336 5
Category
Food
Distribution
20 states
SevereFDA (Food)·F-1365-2022·2022-07-06
Peanut Butter Chocolate Fudge Bars Recalled Due to Salmonella Contamination
Fudgeamentals LLC is recalling Peanut Butter Chocolate Fudge Bars (8 oz.) due to Salmonella contamination in the peanut butter ingredient. 189,096 units were affected nationwide.
Product
PEANUT BUTTER CHOCOLATE FUDGE BAR - 8 oz.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1360-2022·2022-07-06
Snack Fresh Apples and Peanut Butter Fruit Trays Recalled for Salmonella Risk
Stellex/CF Houston, LLC is recalling 134,554 cases of Snack Fresh Apples and Peanut Butter fruit trays (6.5 oz) due to potential Salmonella contamination. Code dates 5/14/21–6/4/22 were distributed across 20 U.S. states.
Product
Snack Fresh Apples and Peanut Butter Net Wt 6.5 oz. packed in clear plastic non-flexible package UPC 0 74641 00044 6 six count per case
Category
Food
Distribution
20 states
SevereFDA (Food)·F-1367-2022·2022-07-06
Peanut Butter Chocolate Fudge Bites Recalled for Salmonella Contamination
Fudgeamentals LLC is recalling PEANUT BUTTER CHOCOLATE FUDGE BITES nationwide due to Salmonella contamination in the peanut butter ingredient. The recall affects 189,096 units.
Product
PEANUT BUTTER CHOCOLATE FUDGE BITES (24-8 OZ) FUDGEAMENTALS
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1366-2022·2022-07-06
Chocolate Variety Tray Recalled for Salmonella Contamination in Peanut Butter
Fudgeamentals Variety Tray (16 oz) is being recalled nationwide due to Salmonella contamination in its peanut butter component. Consumers should not consume the product and should discard it.
Product
VARIETY TRAY (16 OZ) (C-CNC-PBC) FUDGEAMENTALS
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1368-2022·2022-07-06
Fudgeamentals Peanut Butter Fudge Bites Recalled for Salmonella Contamination
Fudgeamentals is recalling Peanut Butter Fudge Bites nationwide due to Salmonella contamination in the peanut butter ingredient. Consumers should not consume the affected product.
Product
PEANUT BUTTER FUDGE BITES (24-8 OZ) FUDGEAMENTALS
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1363-2022·2022-07-06
FDA recalls Giant Apples, Pretzels & Celery with peanut butter for Salmonella risk
Stellex/CF Houston is recalling Giant Apples, Pretzels & Celery with peanut butter trays due to potential Salmonella contamination. The recall affects 134,554 cases distributed across 20 states from May 2021 through June 2022.
Product
Giant Apples, Pretzels & Celery with peanut butter Net Wt. 4 oz. packed in clear non-flexible plastic package UPC 6 88267 55369 1
Category
Food
Distribution
20 states
SevereNHTSA·22V477000·2022-07-06
Travel Trailer Brake System Wiring Defect in Forest River Aurora
Forest River Aurora travel trailers (2021-2022) have a brake system defect where the breakaway switch may be incorrectly wired, preventing trailer brakes from activating. Dealers will provide free inspection and repairs.
Product
COACHMEN — COACHMEN, FOREST RIVER CATALINA, AURORA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-1361-2022·2022-07-06
Snack Fresh Apple & Cheese Bites with Crackers recalled for potential Salmonella contamination
Snack Fresh Apple & Cheese Bites with Crackers are being recalled nationwide due to potential Salmonella contamination. Consumers should not consume the product.
Product
Snack Fresh Apple & Cheese Bites with Crackers Net Wt. 4 oz. packed in clear non-flexible plastic package UPC 0 74641 32841 0 six count per case
Category
Food
Distribution
20 states
SevereFDA (Food)·F-1371-2022·2022-07-06
Fudgeamentals Tiger Butter Fudge Bar Recalled for Salmonella
Fudgeamentals LLC is recalling Tiger Butter Fudge Bar (8 oz) nationwide due to Salmonella contamination in the peanut butter ingredient. Affected lot codes: 22059007, 22083006, 22089006, 22130394.
Product
Fudgeamentals TIGER BUTTER FUDGE BAR (8 OZ)
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1370-2022·2022-07-06
Fudge Trio Holiday Fudge Tray Recalled Nationwide for Salmonella Contamination
Fudgeamentals LLC is recalling Marketside and Walmart Fudge Trio Holiday Fudge Trays nationwide due to Salmonella contamination in the peanut butter ingredient. Consumers should discard these products and not consume them.
Product
1. Marketside FUDGE TRIO HOLIDAY FUDGE TRAY - 16 oz. 2. WALMART MKT FUDGE TRIO (6-16 OZ) HOLIDAY FUDGE TRAY FUDGEAMENTALS
Category
Food
Distribution
Distributed nationwide
HighNHTSA·22V464000·2022-07-06
Cummins Recalls 2020-2022 Trailer-Mounted Generator Sets Due to Shutdown Defect
Cummins is recalling 2020-2022 C500D6Re trailer-mounted generator sets because a logic error may prevent them from shutting down, posing burn and shock risks.
Product
CUMMINS POWER GENERATION — CUMMINS POWER GENERATION GENERATOR SET
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1298-2022·2022-07-06
TEG5000 Analyzer displays incorrect PlateletMapping assay results in TEG Manager
Haemonetics' TEG5000 Analyzer displays incorrect PlateletMapping assay values when connected to TEG Manager Software versions 1.1–4.3.1, potentially affecting laboratory test interpretation.
Product
Product Name: TEG5000 Analyzer (07-022, 07-033) with TEG Analytical Software (07-030, 07-031) and TEG Platelet Mapping Assay - PlateletMapping ADP & AA (07-014), PlateletMapping ADP (07-015), PlateletMapping AA (07-016). Issue occurs when Platelet Mapping Assay results…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1172-2022·2022-07-06
Fluticasone Propionate Nasal Spray Recalled Due to Defective Container
Akorn, Inc. is recalling 44,400 bottles of Fluticasone Propionate Nasal Spray nationwide due to a defective container that prevents proper dispensing. Patients should contact their healthcare provider or pharmacist.
Product
Fluticasone Propionate Nasal Spray, USP, 50 mcg, 16 g net fill weight per amber glass bottle, Rx only, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, NY 11701. NDC 50383-700-16
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1385-2022·2022-07-06
Wilton Rainbow Chip Crunch Sprinkles recalled due to milk contamination
Wilton Industries is recalling Rainbow Chip Crunch Sprinkles (5.25 oz) due to milk contamination. The recall affects 6,400 units distributed nationwide and internationally.
Product
Wilton Rainbow Chip Crunch Sprinkles net wt 5.25 oz. item 710-5364
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1300-2022·2022-07-06
Orthopedic Plates Recalled Due to Incorrect Etching and Mislabeling
One lot of DVR Anatomic distal radius orthopedic plates was incorrectly etched during manufacturing and may have been placed into kits labeled as a different plate model. The affected plates were distributed to healthcare facilities nationwide.
Product
DVR Anatomic, Model No. DVRAR. Distal Volar Radius Anatomical Plate System used for the fixation of fractures and osteotomies involving the distal radius.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22E054000·2022-07-06
Cummins Recalls PD7000 Electric Drivetrains Due to Electrical Grounding Defect
Cummins is recalling PD7000 Electric Drivetrains because an improperly grounded air compressor can cause electric shock. Owners will receive a free repair to install a ground strap.
Product
ELECTRICAL SYSTEM:PROPULSION SYSTEM recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1285-2022·2022-07-06
Backup batteries in Avance CS2 anesthesia machines fail prematurely
GE Healthcare is recalling backup batteries in Avance CS2 and CS2 Pro anesthesia machines manufactured after April 1, 2019. Batteries may fail earlier than expected, affecting approximately 6,600 devices worldwide.
Product
Back up batteries in Avance CS2 and Avance CS2 Pro anesthesia devices manufactured on or after April 1, 2019
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1309-2022·2022-07-06
GCX Channel Mounting Accessory Screws May Loosen or Pull Out
Skytron recalls its GCX Channel Mounting Accessory (model H8-300-40-A) because mounting screws may loosen or pull out when used as a monitor mount on surgical booms. Affected units were distributed worldwide.
Product
Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1169-2022·2022-07-06
Methylphenidate Patch Recall: Defective Delivery System and Adhesive Issues
Daytrana (methylphenidate) patches are being recalled due to ripping patches and poor adhesive transfer affecting drug delivery. This Class II recall involves 8,559 cartons distributed nationwide.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1162-2022·2022-07-06
Losartan Potassium tablets recalled for elevated AZIDO impurity
PD-Rx Pharmaceuticals recalled Losartan Potassium 50 mg tablets nationwide due to AZIDO impurity levels exceeding acceptable manufacturing limits. The recall affects 687 bottles across multiple lots.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1304-2022·2022-07-06
HydroSurg Plus Laparoscopic Irrigator recalled for inability to irrigate
Davol HydroSurg Plus Laparoscopic Irrigators cannot provide irrigation. The FDA issued a Class II recall affecting 4,780 units worldwide.
Product
HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, Handle only, with Cojoined Suction and Irrigation Tubing, Catalog number 0026880
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1295-2022·2022-07-06
CV Minor Kit with Nonsterile Component Recalled for Contamination Risk
ROi CPS LLC is recalling 180 CV Minor Kit units due to a nonsterile component accidentally packaged in the sterile kit, posing a contamination and infection risk.
Product
regard Item Number: 800774001, CV00979A - CV Minor Kit, Sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1292-2022·2022-07-06
Medical Device App Records Inaccurate Urinary Flow When Hearing Aids Active
The ProudP Everyday Uroflow Tracker app may record lower-than-actual urination measurements when a hearing aid or AirPods Live Listen feature is active on the same iPhone, due to interference with the app's sound-based measurement system.
Product
ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version 1.2.0 or earlier
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1293-2022·2022-07-06
Sensica Urine Output System recalled for measurement accuracy complaints
C.R. Bard is recalling 457 Sensica Urine Output System units nationwide due to complaints about urine output measurement accuracy.
Product
Sensica Urine Output System
Category
Medical Device
Distribution
Distributed nationwide