State

New Hampshire product recalls

73,718 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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29951–29975 of 78200

SevereFDA (Devices)·Z-2263-2020·2020-06-17
Endologix Ovation iX Abdominal Stent Graft Systems Recalled for Polymer Leak Risk
Endologix is recalling Ovation iX Abdominal Stent Graft Systems because a material weakness may cause polymer leaks during implantation, potentially leading to clinical events.
Product
Ovation iX Abdominal Stent Graft Systems, REF: TV-AB2080-I, TV-AB2080-J, TV-AB2380-I, TV-AB2380-J, TV-AB2680-I, TV-AB2680-J, TV-AB2980-I, TV-AB2980-J, TV-AB3480-I, TV-AB3480-J
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1297-2020·2020-06-17
Fresenius Kabi Recalls Ketorolac Tromethamine Injection Due to Particulate Matter
Fresenius Kabi is recalling specific lots of Ketorolac Tromethamine Injection because particulate matter was found in reserve sample vials.
Product
KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·20138·2020-06-17
Rexair Recalls Rainbow SRX Vacuums Due to Fire and Burn Hazards
Rexair is recalling about 38,000 Rainbow SRX vacuums because the circuit board can spark, posing fire and burn hazards. Two fires have been reported.
Product
Rainbow SRX Vacuums
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2348-2020·2020-06-17
RayStation 8B Software Recall for Dose Calculation Errors
RaySearch Laboratories is recalling RayStation 8B Service Pack 2 software due to a defect in dose calculation algorithms that could underestimate radiation dose.
Product
RayStation 8B Service Pack 2, UDI # 07350002010235 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2340-2020·2020-06-17
RayStation 5 Service Pack 3 Radiation Therapy Software Recalled
RaySearch Laboratories is recalling RayStation 5 Service Pack 3 software due to a dose calculation error that may underestimate radiation dose.
Product
RayStation 5 Service Pack 3, UDI # 07350002010020 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2326-2020·2020-06-17
Canon Medical System Recalls 24 Infinix-8000C Digital Radiography Systems
Canon Medical System is recalling 24 Infinix-8000C digital radiography systems because loose bolts may cause the catheterization table to tilt.
Product
Infinix-8000C with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2342-2020·2020-06-17
RayStation 6 Service Pack 2 Radiation Therapy Software Recalled for Dose Calculation Error
RaySearch Laboratories is recalling RayStation 6 Service Pack 2 software due to a calculation error that could underestimate radiation dose.
Product
RayStation 6 Service Pack 2, UDI # 07350002010075 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1302-2020·2020-06-17
QuVa Pharma Recalls Subpotent Oxytocin Injection Bags
QuVa Pharma is recalling 648 bags of oxyTOCIN 30 Units/500 mL because the product did not contain the active drug.
Product
oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride Injection for IV Use, Rx only, QuVa Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 888-339-0874, NDC 70092-1068-07
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20V359000·2020-06-17
Volkswagen Recalls 2020 Jetta for Loose Front Brake Caliper Bolts
Volkswagen is recalling one 2020 Jetta because front brake caliper bolts may come loose, potentially affecting brake performance and increasing crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN JETTA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2305-2020·2020-06-17
Biomet A.L.P.S. Proximal Humerus Plating System Drill Block Set Screw Recalled
Biomet is recalling A.L.P.S. Proximal Humerus Plating System Drill Block Set Screws because they were distributed without completed design history files or design transfer activities.
Product
A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM DRILL BLOCK SET SCREW, Item Number: 110017551 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2295-2020·2020-06-17
BioFire FilmArray BCID Panel Recalled for False Positive Proteus Results
BioFire Diagnostics is recalling the FilmArray BCID Panel due to an increased risk of false positive Proteus results when used with specific blood culture media.
Product
FilmArray BCID Panel, RFIT-ASY-0126, 30, Rx Only, CE, IVD, UDI: 00815381020086 used with the following BACT/ALERT Blood Culture Bottle Catalog No./Description: 410851/BACT/ALERT¿ FA Plus 410852/BACT/ALERT¿ FN Plus 410853/BACT/ALERT¿ PF Plus 259790/BACT/ALERT¿ SN…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2329-2020·2020-06-17
Intuitive Surgical Recalls IS4000 Sterilization Trays Due to Sterility Breach Risk
Intuitive Surgical is recalling IS4000 stainless steel reprocessing trays because small holes in the sterilization wrap could compromise sterility and increase infection risk.
Product
STAINLESS STEEL REPROCESSING TRAY, 2D CAMERA HEAD, IS4000, Model No. 400499-03 - Product Usage: is designed to enable complex surgery using a minimally invasive approach.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2347-2020·2020-06-17
RayStation 8B Service Pack 1 Recalled for Dose Calculation Error
RaySearch Laboratories is recalling RayStation 8B Service Pack 1 due to a software error that could underestimate radiation dose.
Product
RayStation 8B Service Pack 1, UDI # 07350002010204 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2289-2020·2020-06-17
Elekta Unity Radiation Therapy System Recalled for Legionella Risk
Elekta, Inc. is recalling 32 Unity image-guided radiation therapy systems due to a potential risk of Legionella presence in the machine room heat exchanger condensation collection tray.
Product
Elekta Unity, UDI 05060191071321, Image-guided radiation therapy system - Product Usage: is indicated for radiation therapy treatments and stereotactic radiation treatments of malignant and benign diseases anywhere in the body as determined by a licensed medical practitioner in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2346-2020·2020-06-17
RayStation 8B Software Recall for Dose Calculation Errors
RaySearch Laboratories is recalling RayStation 8B software due to errors in dose calculation algorithms that could underestimate radiation dose.
Product
RayStation 8B, UDI # 07350002010129 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·20137·2020-06-17
HON Recalls Office Chairs Due to Back Breakage and Fall Hazard
HON is recalling specific office chairs because the back can break, posing a fall and injury hazard to users.
Product
HON Office Chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2341-2020·2020-06-17
RayStation 6 Radiation Therapy Software Recalled for Dose Calculation Error
RaySearch Laboratories is recalling RayStation 6 software due to a calculation error that may underestimate radiation dose.
Product
RayStation 6, UDI # 07350002010013 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2343-2020·2020-06-17
RayStation 6 Service Pack 3 Radiation Therapy Software Recall
RaySearch Laboratories is recalling RayStation 6 Service Pack 3 software due to a calculation error that could underestimate radiation dose.
Product
RayStation 6 Service Pack 3, UDI # 07350002010242 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2353-2020·2020-06-17
RayStation 7 Software Recalled for Dose Calculation Errors
RaySearch Laboratories is recalling RayStation 7 software due to errors in dose calculation algorithms that may underestimate radiation dose.
Product
RayStation 7, UDI # 07350002010068 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1290-2020·2020-06-17
Lupin Recalls Lisinopril 5 mg Tablets Due to Product Mix-Up
Lupin Pharmaceuticals is recalling 4,224 bottles of Lisinopril 5 mg tablets because 10 mg tablets were found in the bottles.
Product
LISINOPRIL — LISINOPRIL (LISINOPRIL)
Category
Drug
Distribution
Distributed nationwide
HighCPSC·20140·2020-06-17
Edwards Recalls Mechanical Heat Detectors Due to Fire Alert Failure
Edwards Fire Safety is recalling about 85,000 mechanical heat detectors that may fail to activate during a fire, posing a risk of failure to alert consumers.
Product
Edwards Mechanical Heat Detectors
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2283-2020·2020-06-17
Siemens Atellica CH Enzymatic Creatinine Recalled for Acetaminophen Interference
Siemens Healthcare Diagnostics is recalling Atellica CH Enzymatic Creatinine reagents because acetaminophen metabolites may interfere with test results.
Product
Atellica CH Enzymatic Creatinine_2, Siemens Material Number 11097533, UDI Number 00630414595795 - Product Usage: use in the quantitative determination of creatinine in human serum, plasma, and urine for the diagnosis and treatment of renal disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2338-2020·2020-06-17
Philips Recalls IntelliSpace PACS 4.4 Due to Potential Image Corruption
Philips Healthcare Informatics is recalling 26 units of IntelliSpace PACS 4.4 because images may potentially become corrupt while using the system.
Product
IntelliSpace PACS 4.4, Product number 837507 - Product Usage: intended to be used by trained professionals, including but not limited to physicians, nurses and medical technicians.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·20139·2020-06-17
Republic Wireless Recalls Relay Charging Cables Due to Overheating and Burn Hazards
Republic Wireless is recalling approximately 15,000 Relay charging cables sold between May 2018 and May 2019 because they can overheat and partially melt, posing a burn hazard.
Product
Charging Cable for Relay Screenless Communication Devices
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2282-2020·2020-06-17
Siemens ADVIA Chemistry Enzymatic Creatinine Recalled for Acetaminophen Interference
Siemens is recalling ADVIA Chemistry Enzymatic Creatinine reagents because acetaminophen metabolites may interfere with test results.
Product
ADVIA Chemistry Enzymatic Creatinine_2, Siemens Material Number 10335869, UDI Number 00630414526690 - Product Usage: use in the quantitative determination of creatinine in human serum, plasma, and urine for the diagnosis and treatment of renal disease.
Category
Medical Device
Distribution
Distributed nationwide