State

New Jersey product recalls

73,566 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: 1,249
Severe: 2,939
Most recent: 2026-10-14

Of the 9,773 recalls naming New Jersey we have scored against our rubric, 1,249 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,939 (30%) are Severe.

Which agencies issued them

These figures cover only the 9,773 recalls whose distribution notice names New Jersey specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25876–25900 of 83339

HighFDA (Food)·F-0233-2022·2021-12-08
Tastykake Buttercreme Iced Creme Filled Chocolate Cupcakes Recall for Metal Fragments
Flowers Foods is recalling Tastykake Buttercreme Iced Creme Filled Chocolate Cupcakes due to potential small metal fragments in an ingredient. The recall affects products distributed across multiple states.
Product
Tastykake Buttercreme Iced Creme Filled Chocolate Cupcakes 14.25oz (6-2ct) box UPC 0 25600 00230 8 & 2.375oz package, UPC 0 25600 00004 5
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-0327-2022·2021-12-08
FDA Recalls Hurricane RX Dilation Balloons for Pressure Failure Risk
Boston Scientific is recalling Hurricane RX Dilation Balloons nationwide due to pinhole defects that cause pressure loss or failure to maintain pressure during endoscopic procedures.
Product
HURRICANE RX DILATION BALLOON 10MM 4CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545960
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0331-2022·2021-12-08
Siemens Dimension Vista 500 software issue affects test accuracy
Siemens is recalling 1,326 Dimension Vista 500 diagnostic devices worldwide due to incorrect default hemolysis, icterus, and lipemia indices that may affect test result accuracy.
Product
Dimension Vista 500- In-vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting, mixing, heating, and measuring spectral intensities to determine a variety of analytes in human body fluid SMN: 10284473 (US) and 10488224 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0315-2022·2021-12-08
INBONE Total Ankle System recalled for package-labeling mismatch
Wright Medical Technology is recalling INBONE Total Ankle System implants because the package contents and package labeling do not match.
Product
INBONE Total Ankle System, INBONE POLY INSERT SZ 2 10mm SULCUS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0259-2022·2021-12-08
Shirley's Choc Whoopie Pie Base recalled for metal contamination
Puratos Corporation is recalling Shirley's Choc Whoopie Pie Base because the product may contain metal foreign material. Affected batches were distributed to customers in multiple U.S. states and internationally.
Product
Shirley's Choc Whoopie Pie Base MB Bg50#
Category
Food
Distribution
11 states
HighFDA (Food)·F-0261-2022·2021-12-08
Shirley's Red Velvet WhoopiePie Recalled for Metal Contamination
Puratos Corporation is recalling Shirley's Red Velvet WhoopiePie MB Bg 50# due to potential metal contamination. The product was distributed to customers across multiple U.S. states and foreign locations.
Product
Shirley's Red Velvet WhoopiePie MB Bg 50#. Material #4107554
Category
Food
Distribution
11 states
HighFDA (Food)·F-0234-2022·2021-12-08
Tastykake Chocolate Cupcakes Recalled for Potential Metal Fragments
Flowers Foods is recalling Tastykake Chocolate Cupcakes 12.75oz boxes due to the potential presence of small metal fragments in an ingredient. The product was distributed across 36 U.S. states.
Product
Tastykake Chocolate Cupcakes 12.75oz, UPC 0 25600 00219 3
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-0320-2022·2021-12-08
Boston Scientific Hurricane RX Dilation Balloons Recalled for Pressure Loss Defect
Boston Scientific is recalling specific lots of Hurricane RX Dilation Balloons due to a pinhole defect that causes pressure loss, resulting in prolonged endoscopic procedures. Affected devices are used for dilating strictures in the bile duct.
Product
HURRICANE RX DILATION BALLOON 4MM 2CM-for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545890
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0322-2022·2021-12-08
Hurricane RX Dilation Balloon Recalled for Pressure Loss Defect
Boston Scientific is recalling the Hurricane RX Dilation Balloon due to a pinhole defect causing pressure loss during endoscopic procedures. The defect may result in prolonged procedures and inability to effectively treat biliary strictures.
Product
HURRICANE RX DILATION BALLOON 6MM 2CM-for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN:M00545910
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0238-2022·2021-12-08
Tastykake Jelly Krimpets recalled for potential metal fragments
Flowers Foods is recalling Tastykake Jelly Krimpets due to potential small metal fragments in an ingredient, as reported by a supplier. The recall affects 12oz and 3oz packages distributed across 37 US states.
Product
Tastykake Jelly Krimpets 12oz (6-2ct) UPC 0 25600 00228 5 & 3oz (3ct) UPC 0 25600 00025 0
Category
Food
Distribution
37 states
HighFDA (Food)·F-0256-2022·2021-12-08
HEB Satin White Layer Cake Mix Recalled for Metal Contamination
Puratos Corporation is recalling HEB Satin White Layer Cake in 50-pound bags due to possible contamination with metal foreign material. The affected product was distributed across multiple U.S. states and internationally.
Product
HEB Satin White Layer Cake Bag 50#. Material #4107393
Category
Food
Distribution
11 states
HighFDA (Devices)·Z-0330-2022·2021-12-08
Dimension Vista 1500 Diagnostic Device: Incorrect HIL Index Defaults
Siemens is recalling 1,407 Dimension Vista 1500 diagnostic devices worldwide due to incorrect default Hemolysis, Icterus, and Lipemia (HIL) index values affecting five assays.
Product
Dimension Vista 1500 In-vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting, mixing, heating, and measuring spectral intensities to determine a variety of analytes in human body fluid SMN: 10444801(US) and 10444802 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0246-2022·2021-12-08
UV-C Germicidal Wand Recalled for Excessive Ultraviolet-C Radiation
MAX LUX CORP is recalling approximately 9900 handheld UV-C germicidal wands (Safe-T Lite) distributed nationwide due to excessive ultraviolet-C radiation emissions.
Product
The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range with an intended use of disinfecting surfaces.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0242-2022·2021-12-08
Target Good & Gather Mixed Berry Sparkling Water Recall for Unlabeled Sulfites
Target Good & Gather Mixed Berry Sparkling Water in 8-packs is being recalled due to unlabeled sulfites. Keurig Dr Pepper discovered the issue after receiving complaints about off flavor and off aroma.
Product
Target Good & Gather Mixed Berry Sparkling Water 8 pack of 12 oz. cans UPC can: 0 85239 11516 9, UPC outer Carton (8 pack): 0 85239 11345 5
Category
Food
Distribution
Distributed nationwide
HighCPSC·22028·2021-12-08
GE Appliances Recalls Free-Standing and Slide-In Ranges for Tip-Over Hazard
GE Appliances is recalling approximately 132,000 free-standing and slide-in electric and gas ranges because they can tip over if a heavy object is placed on an open oven door and the anti-tip-over bracket is not securely installed, risking burn injuries.
Product
Free-Standing and Slide-In Electric and Gas Ranges
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0255-2022·2021-12-08
Finesse Bag 25# Flour Product Recalled for Metal Contamination
Puratos Corporation is recalling Finesse Bag 25# (Material #4107218, Batch Number 10644766) because the product may be contaminated with metal fragments. The product was distributed domestically and internationally.
Product
Finesse Bag 25#. Material #4107218
Category
Food
Distribution
11 states
HighFDA (Devices)·Z-0326-2022·2021-12-08
Boston Scientific HURRICANE RX Dilation Balloon Recalled for Pressure Loss
Boston Scientific is recalling HURRICANE RX Dilation Balloons due to a pinhole defect that causes pressure loss during endoscopic procedures. The device may fail to maintain necessary pressure, potentially prolonging procedures.
Product
HURRICANE RX DILATION BALLOON 10MM 2CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545950
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0241-2022·2021-12-08
Target Good & Gather Coconut Pineapple Sparkling Water Recalled for Unlabeled Sulfites
Keurig Dr Pepper is recalling Target Good & Gather Coconut Pineapple Sparkling Water because some cans contain unlabeled sulfites. The affected products were distributed nationwide.
Product
Target Good & Gather Coconut Pineapple Sparkling Water 8 pack of 12 oz. cans UPC can: 0 85239 04059 1, UPC outer carton (8 pack): 0 85239 03833 8
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0312-2022·2021-12-08
Blood Culture Identification Test Recalled Due to False Positive Risk
BioFire Blood Culture Identification 2 (BCID2) diagnostic panels are being recalled due to increased risk of false positive Acinetobacter calcoaceticus-baumannii results caused by non-viable contamination in blood culture vials.
Product
BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI: 00815381020338 Blood Culture Catalog No./Description: 442023/BD BACTEC Plus Aerobic medium in plastic vials 442021/BD BACTEC Lytic Anaerobic medium in plastic vials 442192//BD BACTEC Plus Aerobic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0328-2022·2021-12-08
Cholesterol test system recalled due to calibration failure
RANDOX CHOL cholesterol test system is recalled due to a calibration defect that causes quality control results to be flagged as out of range. This could result in inaccurate cholesterol measurements in patient samples.
Product
RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol in plasma and serum REF: CH200
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0318-2022·2021-12-08
Blood collection devices recalled due to premature needle retraction
Magnolia Medical Technologies is recalling Steripath Gen2 Blood Collection Systems due to an uptick in complaints of premature needle retraction during blood collection.
Product
The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 Blood Collection System - 21G, Wide Neck 2700-23-EN / Steripath Gen2 Blood Collection System - 23G, Wide Neck 27BD-21-EN / Steripath Gen2 Blood Collection System - 21G, Long…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0239-2022·2021-12-08
7UP Zero Sugar Lemon Lime Soda Recalled for Unlabeled Sulfites
Keurig Dr Pepper is recalling 7UP Zero Sugar Lemon Lime Soda due to unlabeled sulfites detected after customer complaints about off flavor and aroma. The recall affects 9,152 cases distributed nationwide.
Product
7UP Zero Sugar Lemon Lime Soda 12 pack of 12 oz. can UPC Cardboard Wrap Code: 7800001181 UPC Can Code: 0780790
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0262-2022·2021-12-08
Shirley's Sugar Top Muffin Base Recalled for Metal Contamination
Puratos Corporation is recalling Shirley's Sugar Top Muffin Base (15,950 lbs) because the product may contain metal foreign material. The affected batches were distributed to customers in multiple U.S. states and internationally.
Product
Shirley's Sugar Top Muffin Bse MB Bag50#. Material #4107632
Category
Food
Distribution
11 states
HighFDA (Food)·F-0267-2022·2021-12-08
Teg Satin Choc Creme Cake contaminated with metal fragments
Puratos Corporation is recalling Teg Satin Choc Creme Cake (50 lb bags, Batch 10688839) due to possible contamination with metal. The product was distributed across multiple states and internationally.
Product
Teg Satin Choc Creme Cake Bag 50#. Material #4107220
Category
Food
Distribution
11 states
HighFDA (Devices)·Z-0317-2022·2021-12-08
HALYARD STERLING ZERO Nitrile Exam Gloves Recall for Discoloration and Loss of Elasticity
O&M Halyard is recalling HALYARD STERLING ZERO nitrile exam gloves in all sizes due to discoloration and loss of elasticity with aging, making the gloves difficult or impossible to don without tearing. Approximately 5.86 million gloves distributed worldwide are affected.
Product
HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES, Sizes XS, S, M, L, and XL
Category
Medical Device
Distribution
Distributed nationwide