The Recall Desk

State

New Jersey product recalls

73,806 recalls have nationwide distribution and so reach New Jersey. 9,782 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total
9,782
Critical
1,246
Severe
2,944
Most recent
2026-11-04

Of the 9,782 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 2,944 (30%) are Severe.

Which agencies issued them

These figures cover only the 9,782 recalls whose distribution notice names New Jersey specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36201–36225 of 83588

  • SevereFDA (Drugs)·D-0130-2020·2019-10-16

    Morton Grove Recalls Prednisolone Sodium Phosphate Oral Solution Due to Impurity Failure

    Morton Grove Pharmaceuticals is recalling Prednisolone Sodium Phosphate Oral Solution because it failed impurity specifications for Prednisolone Impurity 14.

    Product
    Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL, packaged in a 8 fl oz (237 mL) bottle, Rx only, Manufactured By Morton Grove Pharmaceuticals, Inc., Morton Grove, IL 60053. NDC 60432-212-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V735000·2019-10-16

    Porsche Recalls Cayenne and Panamera for Brake Warning Defect

    Porsche is recalling 2017-2020 Cayenne and Panamera vehicles because the instrument cluster may fail to warn drivers when brake pads are worn out.

    Product
    PORSCHE — PORSCHE CAYENNE, PANAMERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0133-2020·2019-10-16

    DrKids Himasal Nasal Saline Recalled for Potential B. cepacia Contamination

    Unipharma is recalling DrKids Himasal Natural Nasal Saline Solution vials due to a precautionary measure regarding potential contamination with B. cepacia bacteria.

    Product
    DrKids Himasal Natural Nasal Saline Solution, packaged in Pre-measured Singe-Use Vials a) 0.5 mL Each (20 count) UPC 37030244608; b) 1.5 mL Each (20 count) UPC 370302446098, Manufactured in USA by: UNIPHARMA, LLC Tamarac, FL 33321
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V738000·2019-10-16

    BMW Recalls 2020 X3 and X4 Models for Steering Rack Defect

    BMW is recalling 2020 X3 M40i and X4 M40i vehicles because the steering rack pinion teeth may break, causing a loss of steering control.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0049-2020·2019-10-16

    Becton Dickinson Recalls CareFusion MaxPlus Clear Needleless Connectors

    Becton Dickinson is recalling 115,200 CareFusion MaxPlus Clear Needleless Connectors because the valve may fail to close, posing risks of blood loss and air embolism.

    Product
    CareFusion MaxPlus Clear Needleless Connector. Intended for Positive Displacement Connector for needleless access to the IV line and/or IV catheter during IV therapy Cat. No. MP1000-C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V734000·2019-10-16

    Airstream Atlas Motorhomes Recalled for Electrical Wiring Fire Risk

    Airstream is recalling 2019-2020 Atlas motorhomes because incorrect wiring may cause overheating and fire. Dealers will correct the wiring free of charge.

    Product
    AIRSTREAM — AIRSTREAM ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0129-2020·2019-10-16

    Sandoz Recalls Ranitidine Capsules Due to NDMA Impurity Detection

    Sandoz is recalling Ranitidine Hydrochloride Capsules 300mg because a trace amount of the impurity NDMA was detected.

    Product
    Sandoz Ranitidine Hydrochloride Capsules 300mg 30 Capsules Rx Only Manufactured by Sandoz Inc. Princeton, NJ 08540 Product of India NDC 0781-2865-31
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·19V736000·2019-10-16

    Forest River Recalls 2020 RVs for Seatbelt Warning Light Defect

    Forest River is recalling 2020 Sunseeker, Freelander, and Leprechaun vehicles because the seatbelt warning light may not illuminate, increasing crash injury risk.

    Product
    FOREST RIVER — FOREST RIVER LEPRECHAUN, SUNSEEKER, FREELANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0094-2020·2019-10-16

    Centurion Medical CVC Bundle Recall Due to Fluid Droplet Risk

    Centurion Medical is recalling CVC Bundle VanTex kits because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.

    Product
    CVC BUNDLE VANTEX 7F, 3L, 20CM ECVC6065
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0136-2020·2019-10-16

    Pfizer Recalls LMD in Dextrose Bags Due to Sterility Concerns

    Pfizer is recalling 17,832 bags of LMD in Dextrose Injection due to a potential leak that compromises sterility.

    Product
    LMD IN DEXTROSE — LMD IN DEXTROSE (DEXTRAN 40)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0108-2020·2019-10-16

    Roche Tina-quant sTfR Assay Recalled for Rheumatoid Factor Interference

    Roche Diagnostics is recalling Tina-quant sTfR assays due to updated claims regarding rheumatoid factor interference.

    Product
    cobas c 311; cobas c 501, 502,and COBAS INTEGRA 400 plus Analyzer/Module-RF interference claims for the sTfR assay Catalog Number: 20763454122
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0040-2020·2019-10-16

    AZIYO BIOLOGICS Recalls CanGaroo Envelopes Due to Suture Brittleness

    AZIYO BIOLOGICS is recalling CanGaroo Envelopes because sutures may become brittle or break before expiration. The devices are used to secure cardiac and neurostimulator implants.

    Product
    CanGaroo Envelopes labeled as the following: 1. CanGaroo Envelope (Large) (single pack); 2. CanGaroo Envelope (Medium) (single pack); 3. CanGaroo Envelope (Extra Large) (single pack); 4. CanGaroo Envelope (Extra Extra Large) (single pack); 5. CanGaroo…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0031-2020·2019-10-16

    Chef's Companion Chocolate Mousse Mix Recalled for Undeclared Soy

    Diamond Crystal Brands is recalling Chef's Companion Instant Chocolate Mousse Mix because it contains soy lecithin that is not declared on the label.

    Product
    Chef's Companion Instant Chocolate Mousse Mix Net Wt. 1 lb 14 oz (851 g), Dist by Diamond Crystal Brands, Inc. Savannah, GA packaged 8 boxes per case.
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-0106-2020·2019-10-16

    Centurion Medical Products Recalls Triple Lumen CVC Kits Due to Connector Defect

    Centurion Medical Products is recalling Triple Lumen CVC kits because the included BD MaxZeroNeedleess Connector may allow fluid droplets to separate from the sealed surface after disconnection.

    Product
    TRIPLE LUMEN CVC 20CM BUNDLE STCVC2040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0100-2020·2019-10-16

    Centurion Medical Products Recalls OR VANTEX Kits Due to Connector Defect

    Centurion Medical Products is recalling OR VANTEX kits because the included BD MaxZeroNeedleess Connector may allow fluid droplets to separate after disconnection.

    Product
    OR VANTEX 7FR 3L 16CM CVC ECVC6665
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0135-2020·2019-10-16

    Epic Pharma Recalls Estradiol Tablets Due to Foreign Tablet Presence

    Epic Pharma is recalling Estradiol 0.5 mg tablets because 1 mg tablets were found in the bottles. Patients should stop using the product and contact their healthcare provider.

    Product
    ESTRADIOL — ESTRADIOL (ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0096-2020·2019-10-16

    Centurion CVC Insertion Bundle Recalled for Fluid Droplet Risk

    Centurion Medical Products is recalling CVC Insertion Bundles because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.

    Product
    CVC INSERTION BUNDLE 8.5FR 4L 16CM ECVC6355
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0092-2020·2019-10-16

    Centurion CVC Bundle Recall Due to Fluid Droplet Risk

    Centurion Medical Products is recalling CVC bundles containing BD MaxZeroNeedleess Connectors due to a risk of fluid droplets separating from the connector surface.

    Product
    CVC BUNDLE, 20CM, 3L, PI ECVC5120A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0107-2020·2019-10-16

    Centurion Medical UVC Tray Recall Due to Fluid Droplet Risk

    Centurion Medical Products is recalling UVC Trays containing BD MaxZeroNeedleess Connectors due to a risk of fluid droplets separating from the connector surface.

    Product
    UVC TRAY UVT875
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0105-2020·2019-10-16

    Centurion Medical Invasive Procedure Tray Recall for Connector Defect

    Centurion Medical Products is recalling Invasive Procedure Trays because they include a recalled connector that may release fluid droplets.

    Product
    INVASIVE PROCEDURE TRAY MNS9510
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0054-2020·2019-10-16

    Becton Dickinson Recalls BD Microtainer Z Tubes Due to Damaged Reservoirs

    Becton Dickinson & Company is recalling BD Microtainer Z No Additive Tubes because damaged reservoirs may cause insufficient sample volumes and erroneous test results.

    Product
    BD Microtainer Z (No Additive Tubes) Part/Catalog No.365963
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0091-2020·2019-10-16

    Centurion Medical CVC Bundle Recall Due to Fluid Droplet Risk

    Centurion Medical Products is recalling CVC bundles containing a recalled BD connector due to potential fluid droplet separation.

    Product
    CVC BUNDLE, 20CM, 3L, PI ECVC5120
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0062-2020·2019-10-16

    GE Healthcare Recalls AIR Technology Anterior Array MRI Coils

    GE Healthcare is recalling 22 AIR Technology Anterior Array MRI coils because the outer seam may separate, exposing porous internal material that cannot be disinfected.

    Product
    AIR Technology Anterior Array, Catalogue Numbers: (a) 5746694, (b) 5746695, (c) 5746696, a receive-only RF coil designed for use with GE 3.0T MRI systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0078-2020·2019-10-16

    Centurion Neonatal Procedure Tray Recall Due to Connector Fluid Droplet Risk

    Centurion Medical Products is recalling Neonatal Procedure Tray PICC Catheters because the included BD MaxZeroNeedleess Connector may release fluid droplets when disconnected.

    Product
    NEONATAL PROCEDURE TRAY PICC CATHETERS CVI4535
    Category
    Medical Device
    Distribution
    Distributed nationwide