The Recall Desk

State

New Jersey product recalls

73,584 recalls have nationwide distribution and so reach New Jersey. 9,773 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total
9,773
Critical
1,246
Severe
2,942
Most recent
2026-10-14

Of the 9,773 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 9,773 recalls whose distribution notice names New Jersey specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26876–26900 of 83357

  • HighFDA (Devices)·Z-2463-2021·2021-09-22

    BD Gravity IV needle-free connector valve occlusion risk

    BD Gravity IV needle-free connector valves may develop flow issues and partial or total occlusions that could delay therapy. The recall affects 24,360 units distributed worldwide.

    Product
    BD Gravity IV Set 3-port Closed Manifold Back Check Valve 3 Needle-Free Y-sites, REF: CM42500E-07; BD Gravity IV Set 3-port Closed Stopock Manifold Back Check Valve 2 Needle-Free Y-sites, REF: CS42522E-07; BD GRAVITY 10 DP V/NV CHECK VALVE 3-WAY STOPCOCK 4 Smartsite VALVES &…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2445-2021·2021-09-22

    Radiation Therapy Software Risk: Data Loss in Treatment Planning

    Siemens radiation therapy planning software may lose data when editing treatment structures. Incomplete structure sets could be sent to the treatment planning system, affecting treatment plan accuracy.

    Product
    syngo.via RT Image Suite with syngo.via VB30, VB40, VB50 and VB60- Intended for Radiation Therapy Treatment Material Number: 10496180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2471-2021·2021-09-22

    Siemens ACUSON Juniper ultrasound system recalled for intermittent power supply failure

    Siemens Medical Solutions USA is recalling 15 ACUSON Juniper Diagnostic Ultrasound Systems worldwide due to intermittent power supply failures that render the devices inoperable. No injuries or illnesses have been reported.

    Product
    ACUSON Juniper Diagnostic Ultrasound System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2474-2021·2021-09-22

    Philips Allura Xper X-ray imaging system failures at 480V power supply

    Four Philips Allura Xper X-ray imaging systems may fail prematurely when powered at 480V hospital mains, causing coil overheating and reduced imaging performance.

    Product
    The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures. This includes, e.g., peripheral, cerebral, thoracic and abdominal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2468-2021·2021-09-22

    BD Needle-Free Bag Access Valves Recalled for Flow Obstruction

    BD SmartSite needle-free valves may become obstructed, preventing proper fluid flow in medical infusions. The FDA recalls over 295,000 units due to risk of therapy delays.

    Product
    BD SmartSite Bag Access Device Needle-Free Valve, REF: 2300E; BD Bag access Device with 1 Check Valve And Needle Free Valve, REF: 2309E-0006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2475-2021·2021-09-22

    Philips Allura Xper Imaging System Overheating and Malfunction Recall

    Philips Allura Xper imaging systems may fail early when supplied with 480V, causing coil overheating and burning smell. When the system fails, X-ray imaging capability is reduced to emergency mode only.

    Product
    The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures. This includes, e.g., peripheral, cerebral, thoracic and abdominal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2451-2021·2021-09-22

    FDA Recalls Luminex Verigene Enteric Pathogen Test Kits for False Positive Results

    Luminex Corporation is recalling 4,579 Verigene EP Amplification Reagent Kit Test units worldwide due to potential for false positive results. Affected kits distributed across the United States, Austria, France, Greece, Japan, and Turkey may produce incorrect test results.

    Product
    Verigene EP Amplification Reagent Kit Test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2458-2021·2021-09-22

    BD needle-free connector valves may occlude or restrict fluid flow

    BD Burette Gravity Set needle-free connector valves may fail to flush or develop blockages, potentially delaying patient therapy. Lot 21015553 consists of approximately 630 units distributed worldwide.

    Product
    BD BURETTE GRAVITY SET 60 DROP 2 Smartsite VALVES VENTED/NONVENTED, REF: 42163E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0979-2021·2021-09-22

    Vita Aid SynerClear Vanilla Powder Recalled for Undeclared Milk

    Naturo Aid Pharmaceutical Inc. is recalling Vita Aid SynerClear (Vanilla) powder because it may contain undeclared milk residue. Consumers with milk allergies are at risk.

    Product
    Vita Aid SynerClear (Vanilla), VA-924. The product is a powder, packaged in a plastic bottle and a white cap, with a net weight of 650g.
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2461-2021·2021-09-22

    BD SmartSite Bag Access Device Recalled for Valve Occlusion Issues

    CAREFUSION is recalling BD SmartSite Bag Access Device needle-free connector valves due to potential occlusions and flow issues that could delay therapy delivery.

    Product
    BD SmartSite Bag Access Device, REF: 2300E-0500; BD BAG ACCESS DEVICE CHECK VALVE SmartSite VALVE, REF: 2309E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V735000·2021-09-22

    2020-2021 Ford Explorer and Lincoln vehicles rearview camera display failure

    Ford and Lincoln are recalling 228,297 vehicles with 360-degree cameras because the rearview camera image may fail to display, reducing rear visibility and increasing crash risk.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V734000·2021-09-22

    2022 Toyota Prius engine control software may disable hybrid system

    Toyota is recalling 2022 Prius and Prius Prime vehicles whose Engine Control Unit software may falsely trigger shutdown of the hybrid system, causing loss of drive power. Contact Toyota at 1-800-331-4331 for a free software update.

    Product
    TOYOTA — TOYOTA PRIUS PRIME, PRIUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2481-2021·2021-09-22

    Leica BOND Primary Antibody CDX2 Recalled for Performance Specification Issue

    Leica Microsystems recalls BOND Ready-To-Use Primary Antibody CDX2 (PA0375, Lot 69909) because the product may not perform as specified in its instructions for use. The recall affects 237 units distributed nationwide.

    Product
    BOND Ready-To-Use Primary Antibody CDX2 (EP25), REF PA0375
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0801-2021·2021-09-22

    Glycopyrrolate Injection Recalled for Failed Impurities and Degradation Specifications

    Meitheal Pharmaceuticals is recalling Glycopyrrolate Injection, USP 4mg per 20mL in 20mL multi-dose vials due to failed impurities and degradation specifications. The recall affects specific lots distributed nationwide in the USA and India.

    Product
    Glycopyrrolate Injection, USP 4mg per 20mL, 20 mL Multi-Dose Vials, Rx only, Mfd for Meitheal Pharmaceuticals, Chicago, IL 60631. NDC 71288-408-21
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0802-2021·2021-09-22

    Betamethasone Dipropionate Lotion recalled for unknown impurity

    Akorn, Inc. is recalling Betamethasone Dipropionate Lotion USP (Augmented), 0.05%, due to an unknown impurity found in the product that exceeds specification limits. The affected lots were distributed nationwide.

    Product
    Betamethasone Dipropionate Lotion USP (Augmented), 0.05%, packaged in a) 30 mL bottle (NDC 61748-480-30), b) 60 mL bottle (NDC 61748-480-60), Rx only, Manufactured by: Hi-Tech Pharmacal Co. Inc., Amityville,NY 11701
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0799-2021·2021-09-22

    Kroger 70% Isopropyl Alcohol Bottles Mislabeled; Contains Hydrogen Peroxide

    Vi-Jon, Inc. is recalling Kroger 70% Isopropyl Rubbing Alcohol due to a labeling mix-up. The bottles are labeled as isopropyl alcohol but contain Hydrogen Peroxide 3% instead.

    Product
    70% ISOPROPYL RUBBING ALCOHOL — 70% ISOPROPYL RUBBING ALCOHOL (ISOPROPYL RUBBING ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0798-2021·2021-09-22

    Candesartan Cilexetil tablets recalled for impurity specification failure

    Viatris is recalling Candesartan Cilexetil Tablets, USP 16 mg due to failed impurities and degradation specifications. One lot distributed nationwide does not meet required purity standards.

    Product
    CANDESARTAN CILEXETIL — CANDESARTAN CILEXETIL (CANDESARTAN CILEXETIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V731000·2021-09-21

    Workhorse Recalls 2020-2021 C1000 and C650 Vehicles for Safety Standard Failures

    Workhorse Group is recalling 2020-2021 C1000S, C1000M, and 2020 C650 vehicles because they fail to meet multiple Federal Motor Vehicle Safety Standards, increasing the risk of injury, crash, or fire.

    Product
    WORKHORSE MOTOR WORKS — WORKHORSE MOTOR WORKS C1000S, C1000M, C650
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V728000·2021-09-21

    2019-2021 RAM PROMASTER CITY turn signal failure safety recall

    Certain 2019-2021 RAM PROMASTER CITY vehicles may experience turn signal light failures that do not change their flashing rate, preventing drivers from knowing the signals have failed and increasing crash risk. Dealers will update the Body Controller Module software at no cost.

    Product
    RAM — RAM PROMASTER CITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V729000·2021-09-21

    2021 Jeep Grand Cherokee Rearview Camera Display Software Defect

    A software error in the radio system of certain 2021 Jeep Grand Cherokee L vehicles may prevent the rearview camera from displaying, reducing rear visibility and increasing crash risk.

    Product
    JEEP — JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V727000·2021-09-17

    Hyundai Recalls 2017 Sonata Hybrid and Tucson for Engine Bearing Wear

    Hyundai is recalling 2017 Sonata Hybrid and Tucson vehicles because engine connecting rod bearings may wear prematurely, potentially causing engine damage, fire, or stalling.

    Product
    HYUNDAI — HYUNDAI SONATA HYBRID, TUCSON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V726000·2021-09-17

    DRV Recalls 2021 Mobile Suites Trailers Due to Brake Bolt Issues

    DRV Suites is recalling 2021 Mobile Suites and Mobile Suite fifth wheel trailers because improperly tightened brake rotor bolts may loosen or fall off.

    Product
    DRV — DRV MOBILE SUITES, MOBILE SUITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V725000·2021-09-17

    Kia Recalls 2015-2017 Sedona for Turn Signal Software Defect

    Kia is recalling 2015-2017 Sedona vehicles because a software defect may cause turn signals to activate in the opposite direction, increasing crash risk.

    Product
    KIA — KIA SEDONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V723000·2021-09-17

    Forest River Recalls 2022 Coachmen Aurora Travel Trailers for Incorrect Tires

    Forest River is recalling 2022 Coachmen Aurora travel trailers because they were manufactured with incorrect tire sizes. The wrong tires can become overloaded, increasing the risk of a crash.

    Product
    COACHMEN — COACHMEN AURORA
    Category
    Vehicle
    Distribution
    Distributed nationwide