The Recall Desk

State

New Jersey product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33201–33225 of 83518

  • ModerateFDA (Devices)·Z-1783-2020·2020-04-29

    Degania Temperature Sensing Foley Catheters Recalled for Inspection Failures

    Degania Medical Devices is recalling specific lots of temperature sensing Foley catheters due to inadequate incoming inspection practices for the thermistor sensors.

    Product
    Temperature Sensing 100% Silicone Foley Catheter, Part Number 102201101663MD - Product Usage: is a 3 lumen silicone catheter with a sensor to measure temperature while draining the urinary bladder.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1737-2020·2020-04-29

    Boston Scientific Recalls Stretch VL Ureteral Stent Sets Due to Tracking Issues

    Boston Scientific is recalling 57 units of Stretch VL Ureteral Stent Sets because they may be difficult to track over a guidewire, potentially delaying procedures.

    Product
    Stretch VL Ureteral Stent Set 4.8FX22-30CM with .035 Sensor UPN: M006185155080
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1762-2020·2020-04-29

    Olympus Pleuravideoscope Recalled Due to Missing Compatibility Data

    Olympus Corporation of the Americas is recalling 265 Pleuravideoscope Model LTF-160 units because data validating compatibility with certain endo-therapy devices was missing.

    Product
    Olympus Pleuravideoscope, Model LTF-160
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1753-2020·2020-04-29

    Rayner RaySert PLUS Intraocular Lens Injector Recall for Labeling Error

    Rayner Intraocular Lenses Limited is recalling RaySert PLUS RSP01 injectors due to a mismatch between the outer and inner tray expiration dates and lot numbers.

    Product
    RaySert PLUS RSP01. LOT K030. Expiry of 2024-01 - Product Usage: The single use injectors (Model STWOl and Model RSPOl) are intended to be used to compress and insert into the capsular bag only those intraocular lenses that allow the use of these injectors in their approved…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1743-2020·2020-04-29

    Fentanyl Reagent Kit Recalled for Mislabeling as Clinical Diagnostic

    Carolina Liquid Chemistries Corp is recalling Fentanyl Reagent Kits sold to clinical labs without FDA clearance. The products were mislabeled for diagnostic use but are intended for forensic use only.

    Product
    Fentanyl Reagent Kit, Product N. CC444, Contains: FENT R1 Reagent and FENT R2 Reagent
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1728-2020·2020-04-29

    Abbott Recalls Architect HAVAB G Reagent Kits Due to Antigen Concentration Error

    Abbott is recalling 7,347 Architect HAVAB G Reagent Kits because an erroneous concentration value was used during manufacture, resulting in a decreased amount of antigen.

    Product
    ARCHITECT HAVAB G Reagent Kit. List Number 6L27 25.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1763-2020·2020-04-29

    Olympus Pleuravideoscope Recalled Due to Compatibility Data Gaps

    Olympus is recalling 265 Pleuravideoscope units because data validating compatibility with certain endo-therapy devices was missing. Updated manuals are being provided.

    Product
    Olympus Pleuravideoscope, Model LTF-240
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1749-2020·2020-04-29

    Fresenius 2008T BlueStar Hemodialysis Machines Recalled for USB False Alarm

    Fresenius Medical Care is recalling 15,342 hemodialysis machines because a false alarm may appear when a USB device is connected.

    Product
    Fresenius 2008T BlueStar Hemodialysis Machine Part Number Description: 191124 2008T HD SYS. CDX BLUEST AR; 191126 2008T HD SYS. CDX W/BIBAG BLUEST AR; 191128 2008T HD SYS. W/O CDX BLUEST AR; 191130 2008T HD SYS. W/O CDX W/BIBAG BLUEST AR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1744-2020·2020-04-29

    Acuvue Oasys for Astigmatism Contact Lenses Recalled for Package Integrity Failure

    Johnson & Johnson Vision Care is recalling specific Acuvue Oasys for Astigmatism contact lenses due to a package integrity failure found during routine testing.

    Product
    ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G. Base Curve 8.6, Refractive Power -3.00D-1.25/90.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1787-2020·2020-04-29

    Degania Recalls Temperature Sensing Foley Catheters Due to Inspection Failures

    Degania Medical Devices is recalling 9,137 temperature sensing Foley catheters because inadequate incoming inspection practices were used on the thermistor sensors.

    Product
    Temperature Sensing 100% Silicone Foley Catheter, Part Number 102203101463DO - Product Usage: is a 3 lumen silicone catheter with a sensor to measure temperature while draining the urinary bladder.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1751-2020·2020-04-29

    Beckman Coulter Recalls Synchron Opiate 2000 ng Reagent Due to Cross-Reactivity

    Beckman Coulter is recalling Synchron Opiate 2000 ng Reagent because cross-reactivity testing may not meet instructions for use, potentially causing false positive or negative urine test results.

    Product
    Synchron Systems Opiate 2000 ng Reagent (OP2 1 x 250); catalogue no. 475006 for use in conjunction with UniCel DxC 600/800 System(s) and SYNCHRON Systems Drugs of Abuse Testing (DAT) Urine Calibrators. The assay provides a rapid screening procedure for presence of the analyte…
    Category
    Medical Device
    Distribution
    34 states
  • ModerateFDA (Devices)·Z-1739-2020·2020-04-29

    Boston Scientific Recalls Stretch VL Ureteral Stent Sets Due to Tracking Issues

    Boston Scientific is recalling 40 units of Stretch VL Ureteral Stent Sets because they may be difficult to track over a guidewire, potentially delaying procedures.

    Product
    Stretch VL Ureteral Stent Set 7FX22-30CM with .035 Sensor UPN: M006185157080
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V236000·2020-04-28

    Triumph Recalls Motorcycles Due to Front Brake Pad Corrosion Risk

    Triumph is recalling 3,709 motorcycles because front brake pads may corrode and detach, increasing stopping distance and crash risk.

    Product
    TRIUMPH — TRIUMPH XRX (LRH), STREET TRIPLE RS, SPEED TRIPLE RS, SPEED TRIPLE S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V238000·2020-04-28

    Jayco Recalls 2020 Jay Flight SLX Trailers Due to Propane Leak Risk

    Jayco is recalling 2020 Jay Flight SLX travel trailers because an improperly tightened propane hose may leak, increasing the risk of fire or explosion.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT SLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V237000·2020-04-28

    Forest River Recalls 2020 StarTrans PS2 Buses for Seat Belt Defect

    Forest River is recalling 2020 StarTrans PS2 transit buses because seat belt retractors may not secure occupants properly, increasing injury risk in crashes.

    Product
    STARTRANS — STARTRANS PS2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V233000·2020-04-27

    MCI J4500 and J3500 Motor Coaches Recalled for Brake Hose Defect

    Motor Coach Industries is recalling 2014-2019 J4500 and 2018-2019 J3500 motor coaches because brake hoses may crack, causing air leaks and increased stopping distances.

    Product
    MCI — MCI J4500, J3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V234000·2020-04-27

    Blue Bird Recalls School Buses for Parking Brake Defect

    Blue Bird is recalling 2006-2021 Vision and 2007-2013 All American school buses because the parking brake may fail to hold the vehicle on an incline.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION, VISION TRANSIT BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V235000·2020-04-27

    Blue Bird Recalls 2009-2019 Vision Buses for Parking Brake Defect

    Blue Bird is recalling 2009-2019 Vision transit buses because the floor-mounted parking brake may fail to hold the vehicle on an incline when fully loaded.

    Product
    BLUE BIRD — BLUE BIRD VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E026000·2020-04-24

    Denso Fuel Pump Recall for Potential Engine Stall Risk

    Denso is recalling certain fuel pumps where an impeller may crack and deform. This defect can cause the engine to stall while driving, increasing the risk of a crash.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E025000·2020-04-24

    Ford Recalls Replacement Headlamps for 2013-2016 Lincoln MKZ Vehicles

    Ford is recalling specific replacement headlamps for 2013-2016 Lincoln MKZ vehicles because they may have improper beam patterns and missing markings, potentially reducing visibility.

    Product
    LINCOLN — LINCOLN MKZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20112·2020-04-23

    Leviton Recalls 50-Ampere Electrical Connectors Due to Shock Hazard

    Leviton is recalling approximately 98,000 50-ampere electrical connectors, plugs, receptacles, and inlets sold in the US and Canada due to mislabeled terminal markings that pose an electrical shock hazard.

    Product
    Leviton 50 ampere, non-NEMA electrical connectors, plugs, receptacles and inlets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V231000·2020-04-23

    McLaren Recalls 2,763 Vehicles for Fuel Tank Corrosion Risk

    McLaren is recalling 2,763 vehicles because a foam pad may corrode the fuel tank, potentially causing a leak and fire risk.

    Product
    MCLAREN — MCLAREN 570 GT, SENNA, 720S, GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20738·2020-04-23

    LUS Recalls Hair Dryers Due to Electrocution or Shock Hazard

    LUS Distribution Inc. is recalling approximately 2,700 hair dryers and diffusers sold in the U.S. because they lack immersion protection, posing an electrocution or shock hazard if they fall into water.

    Product
    LUS Hair Dryers & Diffusers
    Category
    Consumer Product
    Distribution
    Distributed nationwide