State

New Hampshire product recalls

73,372 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 73,372 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18726–18750 of 77844

HighFDA (Devices)·Z-0371-2023·2022-12-14
2.5 mm LifePort Endotracheal Tube Adapters Deformation Risk
Bunnell's 2.5 mm LifePort Endotracheal Tube Adapters may deform due to improper packaging, potentially affecting ventilator performance. The defect may lead to hypercarbia, hypoxia, and gas trapping.
Product
2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube Adaptors inside Patient Circuit Kits, Catalog: 938
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0422-2023·2022-12-14
Getinge Flow-c and Flow-e Anesthesia Systems: Backup Battery Failure Risk
Getinge Flow-c and Flow-e anesthesia systems are recalled due to backup battery defects that may fail during power outages, potentially requiring manual emergency ventilation. 65 units affected in six US states.
Product
Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System (Product Code 6887900)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0462-2023·2022-12-14
Philips MR 7700 System Recalled for Gradient Coil Fire Risk
Philips is recalling 566 MR 7700 MRI systems nationwide. The gradient coil in these systems may overheat and produce fire or smoke.
Product
Philips MR 7700 System, Model Number 782120
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0461-2023·2022-12-14
Philips MRI System Recall Due to Fire and Smoke Risk
Philips SmartPath to Ingenia Elition X MR System models may produce smoke or fire due to gradient coil heat. Recall affects 566 units nationwide.
Product
Philips SmartPath to Ingenia Elition X MR System, Model Numbers 782118, 782132, 782144
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0390-2023·2022-12-14
Carefusion Bipolar Forceps Recalled for Incomplete Instructions for Use
BD is recalling Carefusion V. Mueller Bipolar Forceps due to incomplete Instructions for Use lacking critical content about power supply interface and cleaning procedures.
Product
Carefusion V. Mueller CUSHING BIPOLAR FORCEPS 1.5MM TIP, INSULATED OVERALL LENGTH 7" (180MM), REF F-2002
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0380-2023·2022-12-14
Bipolar Forceps Recalled for Incomplete Instructions for Use
Carefusion bipolar surgical forceps recalled due to incomplete Instructions for Use missing critical content on power supply interface and maintenance procedures. Distributed nationwide and internationally.
Product
Carefusion V. Mueller GERALD BIPOLAR FORCEPS 1.0MM WIDE TIP OVERALL LENGTH 7" (17.8CM) , REF F-1110
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0407-2023·2022-12-14
Bipolar Forceps Recalled for Missing Instructions on Cleaning and Power Supply
CareFusion V. Mueller bipolar forceps (Ref F-5073) recalled due to missing critical instructions for power supply interface and cleaning and maintenance procedures. Users should obtain the complete Instructions For Use from the manufacturer.
Product
CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5073
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0376-2023·2022-12-14
Surgical Bipolar Forceps Recall: Incomplete Instructions for Use
Carefusion is recalling 218 units of surgical bipolar forceps due to incomplete product instructions. The Instructions For Use is missing information about power supply interface and cleaning/maintenance procedures.
Product
Carefusion V. Mueller HARDY BAYONET BIPOLAR FORCEPS WITH STOP, 0.5MM TIP OVERALL LENGTH 8-1/2" (215MM), REF F-1030
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0377-2023·2022-12-14
Carefusion Bipolar Forceps Recalled Due to Incomplete Instructions
Carefusion recalled 84 units of HARDY-STYLE BAYONET BIPOLAR FORCEPS nationwide and internationally due to incomplete Instructions for Use. The distributed documentation is missing information about power supply interface, cleaning, and maintenance procedures.
Product
Carefusion V. Mueller" HARDY-STYLE BAYONET BIPOLAR FORCEPS, 0.5MM TIP, INSULATED OVERALL LENGTH 8-1/2" (215MM) , REF F-1035
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0410-2023·2022-12-14
CareFusion Bipolar Forceps Recalled Due to Missing Instructions for Use
CareFusion V. Mueller bipolar forceps are being recalled because the provided Instructions for Use are missing critical content about power supply interface and cleaning/maintenance. The complete information is available in the manufacturer's full IFU.
Product
CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS, 1.0MM TIP, STRAIGHT MEDIUM OVERALL LENGTH 8-3/4" (225MM), REF F-5126
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0393-2023·2022-12-14
Bipolar forceps recall for incomplete operating and maintenance instructions
Carefusion is recalling neurosurgical bipolar forceps due to incomplete Instructions for Use. The product is missing critical information about power supply interface and cleaning/maintenance procedures.
Product
Carefusion V. Mueller Neuro/Spine JEWELERS BIPOLAR FORCEPS 0.4MM TIP, CURVED, # 7 OVERALL LENGTH 4-3/4" (120MM), REF F-3007
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0394-2023·2022-12-14
Surgical Bipolar Forceps Recalled for Missing Safety Instructions
Carefusion is recalling surgical bipolar forceps due to incomplete instructions for use. The missing information covers power supply interface and cleaning and maintenance procedures.
Product
Carefusion V. Mueller ADSON BIPOLAR FORCEPS 1.0MM TIP OVERALL LENGTH 4-3/4" (120MM), REF F-3010
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0372-2023·2022-12-14
Shoulder Surgical Navigation System Warning for Bone Stability
A warning has been added to the NextAR Shoulder surgical navigation platform advising verification of adequate coracoid bone stability. Inadequate stability could lead to bone fracture during reverse shoulder surgery.
Product
NextAR Shoulder Surgical Technique, Shoulder NextAR RSA Platform, CT based computer-assisted surgical navigation platform used to perform a reverse shoulder arthroplasty on the glenoid
Category
Medical Device
Distribution
7 states
HighNHTSA·22V923000·2022-12-14
2022-2023 Chevrolet Malibu Recalled for Defective Front Impact Bar Weld
General Motors is recalling certain 2022-2023 Chevrolet Malibu vehicles with improperly welded front impact bars. The structural defect may prevent crash sensors from working correctly, increasing the risk of injury in a crash.
Product
CHEVROLET — CHEVROLET MALIBU
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0378-2023·2022-12-14
Bipolar Forceps Recalled for Missing Power Supply and Cleaning Instructions
Carefusion 2200 Inc is recalling 203 units of V. Mueller SEMKIN Bipolar Forceps due to incomplete Instructions for Use. The IFU is missing critical content related to power supply interface and cleaning/maintenance procedures.
Product
Carefusion V. Mueller" SEMKIN BIPOLAR FORCEPS WITH STOP, 0.7MM TIP OVERALL LENGTH 5-1/2" (140MM), REF F-1040
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0419-2023·2022-12-14
LineSider Spinal System Screws Recalled for Potential Weld Separation
Integrity Implants is recalling 1,702 LineSider Spinal System pedicle screws due to potential weld separation between screw head components that could result in device failure.
Product
LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Cannulated. Thoracolumbosacral pedicle screw system; Spinal interlaminal fixation orthosis. Product sold as non-sterile and shipped in protective sterilization trays. Screws can also be shipped…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0374-2023·2022-12-14
Bipolar Surgical Forceps Recalled for Incomplete Instructions for Use
Carefusion is recalling 418 units of bipolar surgical forceps because the provided instructions lack critical content about power supply interface and maintenance. Complete manufacturer instructions are necessary for safe device operation.
Product
CareFusion V. Mueller SCOVILLE-GREENWOOD BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 7-3/4" (195MM) , REF F-1002
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0401-2023·2022-12-14
Bipolar Forceps Recall: Missing Device Use and Maintenance Instructions
CareFusion bipolar forceps recalled due to incomplete Instructions for Use. Missing documentation covers power supply interface and cleaning/maintenance procedures.
Product
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 0.7MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5016
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0356-2023·2022-12-14
Dover Closed Urethral Tray Recalled for Potential Drainage Blockage Risk
Cardinal Health is recalling Dover Closed Urethral Catheter Trays due to potential blockage of the urinary drainage bag inlet port, which may prevent proper urine drainage and increase the risk of urinary retention.
Product
Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 ml) 5ml Catheter Product Code: 2480 Intended for urinary drainage from the bladder of a patient
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0358-2023·2022-12-14
Dover Urinary Catheter Drainage Tray Recall Due to Blockage Risk
Cardinal Health is recalling Dover Closed Urethral Tray urinary drainage systems due to potential blockage of the drainage bag inlet port, which may prevent proper bladder emptying and increase the risk of urinary retention.
Product
Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter 14 Fr/Ch (4.7 mm) Product Code: 3410 Intended for urinary drainage from the bladder of a patient
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0418-2023·2022-12-14
Spinal Implant Screws Recalled Due to Potential Weld Failure
LineSider Spinal System screws are recalled due to potential weld separation between components that could cause the Tulip Head to detach from the Screw Shank. The recall affects 1,227 screws distributed nationwide.
Product
LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Thoracolumbosacral pedicle screw system; Spinal interlaminal fixation orthosis. Product sold as non-sterile and shipped in protective sterilization trays. Screws can also be shipped…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0413-2023·2022-12-14
Bipolar Forceps Recall: Incomplete Instructions for Surgical Device
BD recalls CareFusion bipolar forceps (Ref F-5301) due to incomplete Instructions For Use. The IFU is missing information about power supply interface and cleaning and maintenance.
Product
CareFusion V. Mueller TITANIUM BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS 1.5MM TIP, STRAIGHT, INSULATED OVERALL LENGTH 8-3/4" (225MM), REF F-5301
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0359-2023·2022-12-14
Dover Closed Urethral Tray Recalled Due to Drainage Port Blockage Risk
Cardinal Health recalls Dover Closed Urethral Tray due to potential blockage of the urinary drainage bag inlet port that could prevent urine drainage and increase risk of urinary retention if bladders are not emptied timely.
Product
Dover Closed Urethral Tray with Vinyl Catheter Product Code: 3420 Intended for urinary drainage from the bladder of a patient
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0379-2023·2022-12-14
Bipolar Forceps Recall: Missing Device Instructions for Use
Carefusion is recalling bipolar forceps due to missing instructions for use. The corrected instructions address power supply interface, cleaning, and maintenance.
Product
Carefusion V. Mueller SEMKIN BIPOLAR FORCEPS 1.5MM TIP, INSULATED OVERALL LENGTH 6" (150MM), REF F-1045
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0392-2023·2022-12-14
Carefusion Bipolar Forceps Recalled for Incomplete Instructions for Use
Carefusion is recalling the V. Mueller Jewelers Bipolar Forceps due to incomplete Instructions for Use missing power supply interface and cleaning/maintenance instructions. The recall affects 236 units distributed nationwide and internationally.
Product
Carefusion V. Mueller JEWELERS BIPOLAR FORCEPS 0.4MM TIP, STRAIGHT OVERALL LENGTH 4" (100MM), REF F-3000
Category
Medical Device
Distribution
Distributed nationwide