State

New Hampshire product recalls

73,366 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 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18676–18700 of 77838

ModerateCPSC·23717·2022-12-15
Crate and Barrel Thornhill Baby Cribs Recalled for Fall Hazard
Crate and Barrel is recalling about 280 Thornhill baby cribs because mattress support pins can become loose or not fit properly, causing the mattress to fall. The firm received six reports of the mattress support pins not fitting correctly or falling out, though no injuries have been reported.
Product
Thornhill Dark Brown and Natural Baby Cribs
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0330-2023·2022-12-14
Sensititre Medical Device Recall: False Antibiotic Susceptibility Test Results
Remel Inc. is recalling Sensititre HPB1 diagnostic plates that may produce false susceptible results for specific bacteria when tested with seven antibiotics. This could lead to inaccurate susceptibility information affecting clinical treatment decisions.
Product
Thermo SCIENTIFIC, Sensititre HPB1, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0335-2023·2022-12-14
Medical Device Recall: Sensititre Test Produces False Antibiotic Susceptibility Results
Remel Inc. is recalling a diagnostic test that may incorrectly report antibiotic susceptibility in certain Gram-negative bacteria. False results could lead to inappropriate antibiotic treatment.
Product
Thermo SCIENTIFIC, Sensititre STP7F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22V927000·2022-12-14
Audi Recalls 2022 E-Tron GT Models Due to Suspension Strut Defect
Audi is recalling 96 2022 E-Tron GT vehicles because a retaining ring on the front suspension strut may come loose, potentially causing air loss and loss of vehicle control.
Product
AUDI — AUDI E-TRON GT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V926000·2022-12-14
Polestar Recalls 2020-2021 Polestar 1 Vehicles for Battery Fire Risk
Polestar is recalling 2020-2021 Polestar 1 vehicles because defective high-voltage battery cells may overheat and cause a fire. Dealers will replace the cells.
Product
POLESTAR — POLESTAR POLESTAR 1
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0339-2023·2022-12-14
CAIRE Liberator 20 Liquid Oxygen System Recalled for Weld Defects
Caire, Inc. is recalling CAIRE Liberator 20 liquid oxygen system units due to weld penetration inconsistencies discovered during an FDA audit. The manufacturing defect affects 3 units.
Product
CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0327-2023·2022-12-14
Thermo Sensititre diagnostic plate recalled for false susceptibility results
Sensititre diagnostic plates may give false antibiotic susceptibility results for certain bacteria species, potentially affecting treatment decisions. The FDA issued a Class I recall for approximately 1,917 units distributed nationwide.
Product
Thermo SCIENTIFIC Sensititre Plate, GN4F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0332-2023·2022-12-14
FDA Class I Recall: Thermo Sensititre Gram Negative Diagnostic Test Inaccuracy
Thermo Scientific Sensititre CMC7AFLF Gram Negative diagnostic tests may produce false susceptible results for certain bacteria, potentially leading to ineffective antibiotic treatment decisions. The FDA has classified this as a Class I recall.
Product
Thermo SCIENTIFIC, Sensititre CMC7AFLF, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0338-2023·2022-12-14
FDA Class I Recall: CAIRE Liberator 30 Liquid Oxygen System Units
Caire, Inc. is recalling five CAIRE Liberator 30 liquid oxygen system units due to weld defects on the inner bottle that could lead to device failure and loss of oxygen supply to dependent patients.
Product
CAIRE Liberator 30, MODEL 13337403, Liquid Oxygen System Unit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0334-2023·2022-12-14
Sensititre STP6F diagnostic plates may report false antibiotic susceptibility results
Remel's Sensititre STP6F diagnostic plates may produce false susceptible results for Gram-negative bacteria when tested with certain antibiotics, potentially leading to inappropriate treatment decisions.
Product
Thermo SCIENTIFIC, Sensititre STP6F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0337-2023·2022-12-14
Liquid Oxygen System Devices Recalled Due to Weld Quality Issues
Caire Inc. is recalling 70 CAIRE Liberator 45 liquid oxygen systems due to inconsistencies in weld penetration on the inner bottle's longitudinal weld seam discovered during an audit.
Product
CAIRE Liberator 45, MODEL 13262253, Liquid Oxygen System Unit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0328-2023·2022-12-14
Medical Device Recall: Sensititre GN6F May Report False Antibiotic Susceptibility Results
The FDA recalled Sensititre GN6F Gram Negative antimicrobial susceptibility test plates (2,471 units) because they may report false results indicating bacteria are susceptible to certain antibiotics when they are actually resistant.
Product
Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22V928000·2022-12-14
2022 Ford Bronco Airbag Sensors May Not Secure Properly
Ford is recalling certain 2022 and 2021 Bronco vehicles because the side impact sensors may not be properly secured. This could cause airbags to deploy unintentionally or fail to deploy in a crash, increasing injury risk.
Product
FORD — FORD BRONCO
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0333-2023·2022-12-14
Gram-negative antibiotic susceptibility test device recalled for false susceptible results
Sensititre MDRGN3F antibiotic test device may return false susceptible results for certain gram-negative bacteria, risking inappropriate antibiotic treatment. FDA Class I recall issued.
Product
Thermo SCIENTIFIC, Sensititre MDRGN3F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0331-2023·2022-12-14
Medical Diagnostic Plate Recalled for False Antibiotic Susceptibility Test Results
Remel Inc is recalling 588 units of the Sensititre Gram Negative IVD AST diagnostic plate due to false susceptible test results for certain bacteria when tested with specific antibiotics. The defect could lead to incorrect treatment decisions.
Product
Thermo SCIENTIFIC, Sensititre CMC5VGNF, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0336-2023·2022-12-14
Caire Liberator 45 Liquid Oxygen System Recalled for Weld Defects
Caire, Inc. is recalling 10 CAIRE Liberator 45 liquid oxygen system units due to inconsistencies in weld penetration on the inner bottle discovered during an FDA audit.
Product
CAIRE Liberator 45, MODEL 13261699, Liquid Oxygen System Unit
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22E099000·2022-12-14
Williamsen-Godwin Recalls Trailers with Fracturing Steering Arms
Williamsen-Godwin is recalling specific trailers equipped with Smart-Steer 2.0 axles because the steering arm may fracture. This defect can cause parts to separate, increasing the risk of a crash.
Product
STEERING recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0329-2023·2022-12-14
Sensititre GN7F Antibiotic Test Plates Recalled for Inaccurate Susceptibility Results
Remel Inc. recalled 8,073 units of Sensititre GN7F antibiotic susceptibility test plates after discovering they may report false results for certain bacteria, potentially leading to incorrect antibiotic treatment decisions.
Product
Thermo SCIENTIFIC, Sensititre GN7F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0185-2023·2022-12-14
Boston Baking Mini Crumb Cake Recalled for Undeclared Pecan Allergen
Boston Baking Mini Crumb Cake (3 oz, individually wrapped) is recalled for undeclared pecans. The product was distributed in six northeastern states and may pose a serious risk to consumers with tree nut allergies.
Product
Boston Baking Mini Crumb Cake - individually wrapped - 3 oz. Storage Instructions: 10 months frozen, 7 days ambient (Boston Baking case label); Sell-by 5 days after packed-on date (Whole Foods final packaging) - product is distributed frozen
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-0360-2023·2022-12-14
Dover urinary catheter drainage bag occlusion defect nationwide recall
Cardinal Health is recalling Dover urinary catheter trays due to potential blockage of the drainage bag inlet port, which may prevent urine drainage and increase the risk of urinary retention.
Product
Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm), 5 mL Catheter Pre-connected to 1000 mL Drainage Bag Product Code: 3450 Intended for urinary drainage from the bladder of a patient
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0408-2023·2022-12-14
Bipolar Forceps Recalled for Incomplete Instructions for Use
CareFusion bipolar forceps recalled nationwide due to incomplete Instructions for Use missing power supply interface and cleaning information. The missing content could affect proper device operation and maintenance.
Product
CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS, 1.5MM TIP, STRAIGHT STANDARD, 8-3/4" (225MM), REF F-5124
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0373-2023·2022-12-14
Surgical Bipolar Forceps Recalled Due to Missing Operating and Maintenance Instructions
CareFusion is recalling 1369 units of V. Mueller bipolar surgical forceps (Model F-1000) due to incomplete instructions for use. The provided instructions lack information about power supply interface and cleaning and maintenance procedures.
Product
CareFusion V. Mueller CUSHING BAYONET BIPOLAR INSULATED FORCEPS, 0.7MM TIP OVERALL LENGTH 7-1/2" (190MM) , REF F-1000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0405-2023·2022-12-14
Bipolar forceps Instructions for Use missing power supply and maintenance information
CareFusion bipolar forceps have incomplete Instructions for Use missing power supply interface and maintenance guidance. Users should obtain complete instructions from the manufacturer before use.
Product
CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS 0.7MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5067
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0415-2023·2022-12-14
CareFusion Bipolar Forceps Recalled Due to Incomplete Instructions
CareFusion recalls 142 units of bipolar surgical forceps due to incomplete Instructions for Use lacking power supply interface and maintenance guidance found in the manufacturer's version.
Product
CareFusion V. Mueller TITANIUM BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS 1.0MM TIP, STR, MED, INSULATED OVERALL LENGTH 8-3/4" (225MM), REF F-5303
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0397-2023·2022-12-14
Bipolar Surgical Forceps Recalled for Incomplete Instructions for Use
CareFusion bipolar surgical forceps recalled due to incomplete Instructions for Use missing power supply interface and maintenance guidance.
Product
CareFusion V. Mueller euro/Spine TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 8-1/2" (215MM), REF F-5006
Category
Medical Device
Distribution
Distributed nationwide