The Recall Desk

State

New Jersey product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45026–45050 of 83606

  • HighFDA (Devices)·Z-0804-2018·2018-03-07

    ConMed Recalls STAT 2 I.V. Gravity Flow Controllers Due to Inaccurate Flow Rates

    ConMed Corporation is recalling STAT 2 I.V. Gravity Flow Controllers and administration sets because they exhibit inaccurate or inconsistent flow rates.

    Product
    STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary, Secondary Administration Sets and Extension Sets (Catalog Numbers: (1) S2, STAT 2¿ I.V. Controller, (2) S2-12, STAT 2¿ Extension Set Gravity Flow Controller, 12 length, (3) S2-20 MD, STAT 2¿ Secondary Set Gravity Flow…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0696-2018·2018-03-07

    Olympus Recalls Urologic Endoscopic Working Inserts and Bridges Due to Adhesive Fragments

    Olympus is recalling specific urologic endoscopic working inserts and bridges because adhesive fragments may detach and enter patients during procedures.

    Product
    A20975A "Working insert, with ramp, one way" (Lots 13ZW to 172W; A20976A "Bridge, one way" (Lots 146W to 172W) and A20977A "Bridge, two way" (Lots 146W to 174W) Product Usage: A20975A: Working insert for endoscopic diagnosis and treatment in urologic applications. A20976A…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0811-2018·2018-03-07

    NxStage Dialysate Sacks Recalled for Exceeding Endotoxin Quality Standards

    NxStage Medical is recalling dialysate sacks because endotoxin levels may exceed the ANSI/AAMI quality standard of 0.5 EU/ml.

    Product
    NxStage Dialysate Sack: 1) REF SAK-301 UDI-M535SAK3010, 2) REF SAK-302 UDI-M535SAK3020, 3) REF SAK-303 UDI-M535SAK3030, 4) REF SAK-304 UDI-M535SAK3040, 5) REF SAK-306 UDI-M535SAK3060, 6) REF SAK-307 UDI- M535SAK3070, 6) REF SAK-402 UDI-M535SAK4020, 7) REF SAK-405 UDI…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0830-2018·2018-03-07

    Cook Inc. Recalls Percutaneous Gastrostomy Sets Due to Wire Guide Defect

    Cook Inc. is recalling 615 units of Mallinckrodt Institute Percutaneous Gastrostomy Sets because wire guides may be loaded backwards into the holder.

    Product
    Mallinckrodt Institute Percutaneous Gastrostomy Set Product Usage: Intended for the percutaneous placement of a catheter for gastroenteric feeding
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0703-2018·2018-03-07

    Oakworks Medical Imaging Table Foot Controls Recalled for Lodging Hazard

    Oakworks Inc. is recalling foot controls for specific medical imaging tables because they can become lodged under the table base or column.

    Product
    Foot Controls impacted for the following devices: OAKWORKS¿ Medical CFPM 300 Imaging Table OAKWORKS¿ Medical CFPM 301 Imaging Table OAKWORKS¿ Medical CFPM 400 Imaging Table OAKWORKS¿ Medical CFPM 401 Imaging Table OAKWORKS¿ Medical CFPMB 301 Bariatric Imaging Table…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0814-2018·2018-03-07

    Otto Bock Kenevo Knee Joints Recalled for Pylon Breakage Risk

    Otto Bock is recalling 75 Kenevo knee joints due to a design issue that could cause the pylon to break under specific heavy-use conditions.

    Product
    OTTO BOCK Kenevo knee joints Model 3C60
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-0819-2018·2018-03-07

    Accord Media Recalls Ultra Renew Devices for Unapproved LED Light

    Accord Media, LLC is recalling 524 Ultra Renew devices distributed nationwide because they use an unapproved green LED light to treat hyperpigmentation.

    Product
    Ultra Renew
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·18117·2018-03-07

    Topson Downs Recalls Cat & Jack Girls' Jeans Due to Laceration Hazard

    Topson Downs is recalling Cat & Jack Girls' Star Studded Skinny Jeans because metal stars can detach and cause lacerations. Consumers should stop wearing them and return them to Target for a refund.

    Product
    Cat & Jack Girls' Star Studded Skinny Jeans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0721-2018·2018-03-07

    Zimmer Biomet Recalls Segmental System Distal Femur Components

    Zimmer Biomet is recalling 3,350 units of the Segmental System, ZSS Distal Femur, because the products exceeded tested weights, potentially compromising the sterile barrier.

    Product
    Zimmer Segmental System, ZSS Distal Femur. Sizes as follows: a. Size B-LT (Item No. 00585001201); b. Size B-RT (Item No. 00585001202); c. Size C-LT (Item No. 00585001301); d. Size C-RT (Item No. 00585001302) Components of the system are intended to replace the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0832-2018·2018-03-07

    Cook Recalls Wills-Oglesby Percutaneous Gastrostomy Sets Due to Wire Guide Defect

    Cook Inc. is recalling Wills-Oglesby Percutaneous Gastrostomy Sets because wire guides may be loaded backwards into the holder.

    Product
    Wills-Oglesby Percutaneous Gastrostomy Set Product Usage: Intended for the percutaneous placement of a catheter for gastroenteric feeding
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0716-2018·2018-03-07

    Philips Recalls Allura Xper Systems Due to Anode Drive Unit Failure

    Philips is recalling 705 Allura Xper systems because Anode Drive Units may fail in high-voltage regions, reducing X-ray performance to emergency mode.

    Product
    Allura Xper systems with Certeray X-ray Generator located in regions with high mains (480V) voltage. Product Usage: The Allura Xper series is intended for use on human patients to perform: Vascular, cardiovascular and neurovascular imaging applications, including…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0815-2018·2018-03-07

    Otto Bock Kenevo Knee Joints Recalled for Pylon Breakage Risk

    Otto Bock is recalling four Kenevo knee joints due to a design issue that could cause the pylon to break, leading to a fall.

    Product
    OTTO BOCK Kenevo knee joints Model 3C60=ST
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-0694-2018·2018-03-07

    Integra CUSA Clarity Footswitch Recalled for Unintended Activation

    Integra LifeSciences is recalling 155 CUSA Clarity footswitches because a defect may cause unintended ultrasonic fragmentation activation during surgery.

    Product
    Footswitch accessory to the CUSA Clarity Ultrasonic Tissue Ablation System; Catalogue No: C7000 Product Usage: The footswitch is a component of the CUSA Clarity Ultrasonic Surgical Aspirator System, which is indicated for use in surgical procedures where fragmentation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0837-2018·2018-03-07

    M&P Food Productions Recalls Vareniki Potato and Onion for Undeclared Wheat

    M&P Food Productions is recalling Vareniki Potato and Onion because the product contains undeclared wheat. This poses a risk to individuals with wheat allergies or celiac disease.

    Product
    M&P Food Productions brand Vareniki Potato and Onion, Net Wt. 14 oz. (396 g), Keep Frozen, UPC: 7 0 7163 02616 7
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-0702-2018·2018-03-07

    Moog Curlin Infusion Sets Recalled for Particulate Contamination

    Zevex Incorporated is recalling specific lots of Moog Curlin Infusion Administration Sets due to particulate matter found on the spike.

    Product
    MOOG Curlin Infusion Administration Set, Ref 340-4169, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and distal Ultrasite Needleless Injection Port (Positive Pressure), Anti-Siphon Valve included for Free Flow Protection, packaged 20/box, for use with the Moog Curlin…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·18726·2018-03-07

    Husqvarna Recalls FS 450 Competition Motorcycles Due to Brake Failure Hazard

    Husqvarna is recalling approximately 160 FS 450 closed course competition motorcycles from model years 2016 to 2018 because a cracked front brake piston can cause brake failure and crashes.

    Product
    Husqvarna FS 450 closed course competition motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0700-2018·2018-03-07

    Moog Curlin Infusion Sets Recalled for Particulate Matter on Spike

    Zevex Incorporated is recalling Moog Curlin Infusion Administration Sets because particulate matter was found on the spike. The recall covers 7,979 cases distributed nationwide and internationally.

    Product
    MOOG Curlin Infusion Administration Set, Ref 340-4166, Non-DEHP Microbore Tubing with Non-Vented Spike, Anti-Siphon Valve included for Free Flow Protection, packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile. Product Usage…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0692-2018·2018-03-07

    Stryker Recalls Berchtold Chromophare Monitor Arms Due to Weld Defects

    Stryker Communications is recalling 850 Berchtold Chromophare Dual Monitor Carrier Arms and Flat Panels because the mounts may have missing or incomplete welds.

    Product
    Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted Surgical Light System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V157000·2018-03-07

    Thomas Built Buses Minotour Recalled for Wheelchair Lift Safety Defect

    Daimler Trucks North America is recalling 2007-2018 Thomas Built Buses Minotour school buses because the wheelchair lift may operate while the vehicle is in motion.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0805-2018·2018-03-07

    ConMed Recalls STAT 2 I.V. Gravity Flow Sets Due to Inaccurate Flow Rates

    ConMed is recalling STAT 2 I.V. Gravity Flow Needle-Free Controller sets because they exhibit inaccurate or inconsistent flow rates.

    Product
    STAT 2¿ I.V. Gravity Flow Needle-Free Controller Primary Administration Sets and Extension Sets (Catalog Numbers: (1) S2-12 N, STAT 2¿ Extension Set Gravity Flow Controller (Needle-Free), 12 length, (2) S2V-20 N, STAT 2¿ Primary Administration Set Gravity Flow Controller…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0840-2018·2018-03-07

    M&P Food Productions Vareniki Recalled for Undeclared Wheat

    M&P Food Productions is recalling Vareniki - farmer cheese due to undeclared wheat. Consumers with celiac disease or wheat allergies should not consume the product.

    Product
    M&P Food Productions brand Vareniki - farmer cheese, Hand made, Net Wt. 14 oz. (396 g), Keep Frozen, UPC: 7 0716 302618 1
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-0835-2018·2018-03-07

    M&P Food Productions Recalls Vareniki Sour Cherry for Undeclared Allergens

    M&P Food Productions is recalling Vareniki Sour Cherry because the product contains undeclared wheat and Red #40.

    Product
    M&P Food Productions brand Vareniki Sour Cherry, Net Wt. 14oz (396g), Keep Frozen, UPC: 7 07163 02615 0
    Category
    Food
    Distribution
    10 states
  • HighNHTSA·18V154000·2018-03-07

    BMW Recalls 2018 X3 Models for Potential Rear Spoiler Detachment

    BMW is recalling 2018 X3 xDrive30i and M40i vehicles because the rear spoiler may not be properly attached or may be missing screws, posing a road hazard.

    Product
    BMW — BMW X3
    Category
    Vehicle
    Distribution
    Distributed nationwide