State

New Jersey product recalls

73,718 recalls have nationwide distribution and so reach New Jersey. 9,780 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,780
Critical: 1,246
Severe: 2,942
Most recent: 2026-10-28

Of the 9,780 recalls naming New Jersey we have scored against our rubric, 1,246 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,942 (30%) are Severe.

Which agencies issued them

These figures cover only the 9,780 recalls whose distribution notice names New Jersey specifically. The 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28776–28800 of 83498

HighFDA (Devices)·Z-1453-2021·2021-04-28
BIOTRONIK IPERIA 7 ICDs Recalled for Premature Battery Depletion
BIOTRONIK Inc is recalling 2,881 IPERIA 7 ICDs and CRT-Ds due to a potential for premature battery depletion.
Product
BIOTRONIK IPERIA 7, DR-T DF4 ProMRI, REF 392423, UDI: 04035479128913 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V299000·2021-04-28
Suzuki Recalls 2019-2020 UH200 Motorcycles Due to Speedometer Defect
Suzuki is recalling 2019-2020 UH200 motorcycles because corroded speedometer resistors may cause the speedometer and odometer to stop working, increasing crash risk.
Product
SUZUKI — SUZUKI UH200
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1462-2021·2021-04-28
Biotronik ILIVIA Neo 7 VR-T DF-1 ProMRI Recall for Battery Depletion
Biotronik is recalling 74 ILIVIA Neo 7 VR-T DF-1 ProMRI implantable cardioverter defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK ILIVIA NEO 7 VR-T DF-1 ProMRI, REF 429531, UDI: 04035479156763 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1451-2021·2021-04-28
Biotronik ITREVIA 7 Defibrillators Recalled for Premature Battery Depletion
Biotronik is recalling 499 ITREVIA 7 defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK ITREVIA 7, VR-T DF-1, REF 393040, UDI: 04035479129552 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1471-2021·2021-04-28
Smiths Medical Recalls Medex High Pressure Adaptors and LogiCal Kits
Smiths Medical ASD Inc. is recalling specific lots of Medex High Pressure Adaptors and LogiCal Kits due to insufficient or incomplete welds.
Product
Mark 910 LogiCal, Model Number DPS567201. for blood pressure monitoring and blood sampling.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1454-2021·2021-04-28
Biotronik Inventa 7 ICDs Recalled for Premature Battery Depletion
Biotronik is recalling 702 Inventa 7 ICDs due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK INVENTRA 7, HF-T QP DF4 IS4, REF 393012, UDI: 04035479129286 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1455-2021·2021-04-28
Biotronik ITREVIA 7 Defibrillators Recalled for Premature Battery Depletion
Biotronik Inc is recalling 658 ITREVIA 7 implantable defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK ITREVIA 7, DR-T QP DF-1, REF 392412, UDI: 04035479128807 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21119·2021-04-28
Pentair Recalls StaRite and Mastertemp Pool Heaters Due to Fire Hazard
Pentair Water Pool and Spa is recalling about 4,700 StaRite and Mastertemp pool heaters because a connection can leak a combustible air-gas mixture, posing a fire hazard.
Product
StaRite and Mastertemp pool heaters
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21V298000·2021-04-28
2021 BMW 330E Seat Belt Buckle Assembly Bolt Not Properly Secured
BMW is recalling certain 2021 330E, 330i, M340i, and M3 vehicles due to an undertightened bolt on the front seat belt buckle assembly. The defect may prevent proper occupant restraint, increasing injury risk.
Product
BMW — BMW M340I, 330I, 330E, M3
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V300000·2021-04-28
Blue Bird Recalls 2018-2021 School Buses for Power Steering Defect
Blue Bird is recalling 2018-2021 Vision and All American school buses because an electrical issue may cause a loss of power steering, increasing crash risk.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, ALL AMERICAN, VISION, VISION SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1480-2021·2021-04-28
Smiths Medical Recalls Tubing Components Due to Incomplete Welds
Smiths Medical ASD Inc. is recalling specific lots of tubing components for blood-pressure transducers due to insufficient or incomplete welds.
Product
Tubing with male luer lock adapter (Component) a. 76 cm, REF 601280 b. 122 cm, REF 607281. component of extravascular blood-pressure Transducer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1449-2021·2021-04-28
BIOTRONIK IPERIA 7 ICDs Recalled for Premature Battery Depletion
BIOTRONIK Inc is recalling 3,832 IPERIA 7 ICDs and CRT-Ds due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK IPERIA 7,VR-T, DX, DF-1, ProMRI, REF 393032, UDI: 04035479129477 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1456-2021·2021-04-28
Biotronik ILIVIA 7 ICD Recall for Premature Battery Depletion
Biotronik is recalling 3,497 ILIVIA 7 implantable cardioverter defibrillators due to a potential for premature battery depletion. The recall covers units distributed nationwide and worldwide.
Product
BIOTRONIK ILIVIA 7, DR-T DF4 ProMRI, REF 404623, UDI: 04035479142100 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1446-2021·2021-04-28
Biotronik Iperia 7 Defibrillators Recalled for Premature Battery Depletion
Biotronik is recalling 1,652 Iperia 7 defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK Iperia 7, DR-T, DF-1, ProMRI REF 392409, UDI: 04035479128777 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1441-2021·2021-04-28
BIOTRONIK Ilestro 7 DR-T ICDs Recalled for Premature Battery Depletion
BIOTRONIK Inc is recalling Ilestro 7 DR-T implantable cardioverter defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK Ilestro 7 DR-T, DF-1, REF383562, UDI: 04035479125189 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1478-2021·2021-04-28
Smiths Medical Recalls Medex High Pressure Tubing Due to Weld Defects
Smiths Medical ASD Inc. is recalling specific lots of Medex high pressure tubing and components due to insufficient or incomplete welds.
Product
HIGH PRESSURE TUBING, 72IN, Model Number MX152114 (Component). Stopcocks and manifolds are used to control the direction of IV fluid flow.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1470-2021·2021-04-28
Smiths Medical Recalls LogiCal Monitoring Sets Due to Incomplete Welds
Smiths Medical ASD Inc. is recalling specific lots of LogiCal Monitoring Sets and related components due to insufficient or incomplete welds.
Product
LogiCal Monitoring Set, Model Number DPS564898. for blood pressure monitoring and blood sampling.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1458-2021·2021-04-28
Biotronik ILIVIA 7 Defibrillators Recalled for Premature Battery Depletion
Biotronik is recalling 779 ILIVIA 7 defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK ILIVIA 7, VR-T DF4 ProMRI, REF 404626, UDI: 04035479142131 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1461-2021·2021-04-28
Biotronik ILIVIA 7 Defibrillators Recalled for Premature Battery Depletion
Biotronik Inc is recalling 1,547 ILIVIA 7 defibrillators due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK ILIVIA 7, DR-T DF-1 PROMRI, REF 404622, UDI: 04035479142094 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1472-2021·2021-04-28
Smiths Medical Recalls Left Heart Kits Due to Incomplete Welds
Smiths Medical ASD Inc. is recalling specific lots of Left Heart Kits and related components due to insufficient or incomplete welds.
Product
Left Heart Kit, Model Number M20268. for blood pressure monitoring.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1457-2021·2021-04-28
Biotronik ILIVIA 7 ICDs Recalled for Premature Battery Depletion
Biotronik is recalling 914 ILIVIA 7 ICDs due to a potential for premature battery depletion. The devices are distributed nationwide and worldwide.
Product
BIOTRONIK ILIVIA 7, VR-T DF-1 ProMRI, REF 404625, UDI: 04035479142124 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V302000·2021-04-28
2021 Hyundai Elantra seat back recliner frame welding defect
Hyundai is recalling certain 2021 Elantra vehicles because the driver and front passenger seat back recliners may have been improperly welded and could separate during a crash, increasing injury risk.
Product
HYUNDAI — HYUNDAI ELANTRA
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21118·2021-04-28
UST Recalls LifeSeasons Iron Supplement Due to Child-Resistant Packaging Failure
UST Mfg. LLC. is recalling LifeSeasons Blood Nourish-R iron supplements because the bottles do not meet child-resistant packaging requirements, posing a poisoning risk to young children.
Product
LifeSeasons Blood Nourish-R Iron Supplement
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1450-2021·2021-04-28
Biotronik ITREVIA 7 Defibrillators Recalled for Premature Battery Depletion
Biotronik is recalling 386 ITREVIA 7 implantable defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK ITREVIA 7, VR-T DX DF-1, REF 393037, UDI: 04035479129521 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1464-2021·2021-04-28
Biotronik ILIVIA NEO 7 DR-T DF-1 ProMRI Defibrillators Recalled for Battery Depletion
Biotronik is recalling 98 ILIVIA NEO 7 DR-T DF-1 ProMRI defibrillators due to a potential for premature battery depletion.
Product
BIOTRONIK ILIVIA NEO 7 DR-T DF-1 ProMRI, REF 429529, UDI: 04035479156749 - Product Usage: intended to provide ventricular tachycardia pacing and ventricular defibrillation for automatic treatment of life-threatening ventricular arrhythmias.
Category
Medical Device
Distribution
Distributed nationwide