State

New Jersey product recalls

73,106 recalls have nationwide distribution and so reach New Jersey. 9,767 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,767
Critical: 1,249
Severe: 2,486
Most recent: 2026-09-25

Of the 9,767 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 2,486 (25%) are Severe.

Which agencies issued them

These figures cover only the 9,767 recalls whose distribution notice names New Jersey specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12026–12050 of 82873

HighFDA (Food)·F-1291-2024·2024-06-12
Garden Vegetable Cream Cheese Spread recalled for potential Salmonella
Schreiber Foods is recalling Garden Vegetable Cream Cheese Spread sold under multiple brands due to potential Salmonella contamination. Approximately 835,721 units were distributed to 19 states and Puerto Rico.
Product
Garden Vegetable Cream Cheese Spread. Net Wt 8 oz. (226g). Keep Refrigerated, packaged under the following brands: 1. Fareway, UPC 0 21333-83053 9. Packed for Fareway Store, Inc. Boone, Iowa 50036. 2. Essential Everyday, UPC 0 41303-00625 2. Distributed By Supervalu Inc., Eden…
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-1934-2024·2024-06-12
LOSPA Tibial Insert Knee Implant Component Recalled for Unsupported Expiration Date
CORENTEC is recalling LOSPA Tibial Insert knee implant components due to an unsupported 10-year expiration date. Patients with these devices should consult their physician.
Product
LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A Product Description: Tibial Insert
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1968-2024·2024-06-12
Vascular graft slider component may separate from core
Atrium Medical's ADVANTA VXT vascular graft may experience separation of the slider mechanism from its core, affecting over 11,000 US units. No injuries have been reported.
Product
ADVANTA VXT, 6X70, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1300-2024·2024-06-12
Frozen cookie dough products recalled for potential salmonella contamination
Rise Baking Company is recalling frozen cookie dough products sold under Costco, Member's Mark, Panera, and Rise Baking brands due to potential Salmonella contamination. The recall affects 29,019 cases distributed across 21 states.
Product
Costco Chocolate Chunk Frozen Cookie Dough, Net Wt. 33lb (14.97kg), 1.6 oz dough pucks Member's Mark Chocolate Chunk, Net Wt. 14.85lb (6.74kg), 144/1.65 oz dough pucks/case Panera Chocolate Chipper Cookie, Net Wt. 41.25 lb (18.71kg), 220/3 oz dough pucks/case Rise Baking Jumbo…
Category
Food
Distribution
21 states
HighFDA (Devices)·Z-2029-2024·2024-06-12
Hysteroscope recalled due to missed required leakage test
Olympus OES 4000 Hysteroscope Model A4674A is being recalled because a required leakage test was not performed after device repairs. Liquid could enter the eyepiece, causing a foggy image during use.
Product
OES 4000 Hysteroscope, Model/Catalog Number: A4674A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1946-2024·2024-06-12
Newport Laser Systems Recalled for Removable Safety Key Defect
Newport has recalled Class II laser systems because their key-actuated safety switch can be removed while the laser remains on, violating federal safety requirements.
Product
Newport s N-LHP-928(j) units if sold as a laser head/power supply set, and N5-LPL-944-080 and N6-LPL-944-080 if sold as a power supply alone.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2008-2024·2024-06-12
FLIXENE vascular graft recalled for slider separation defect
Atrium Medical recalls FLIXENE vascular grafts due to reported separation between the slider rod and swivel core. Affected grafts may fail to function properly if deployed.
Product
FLIXENE, 7X30, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1965-2024·2024-06-12
Vascular Graft Recall Due to Swivel Rod Separation
Atrium Medical is recalling the ADVANTA VXT vascular graft due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. This component separation could affect device function.
Product
ADVANTA VXT, 6X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1956-2024·2024-06-12
Vascular Graft Slider Component May Separate from Core
Atrium Medical is recalling ADVANTA VXT vascular grafts worldwide after reports of the slider swivel rod separating from the swivel core with a notable gap between components.
Product
ADVANTA VXT, 7X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1992-2024·2024-06-12
Vascular Graft Recalled Due to Swivel Rod Separation Risk
Atrium Medical is recalling ADVANTA VXT vascular grafts worldwide due to complaints of the swivel rod separating from the core, which could compromise device function during medical procedures.
Product
ADVANTA VXT, 6X45, 1GDS, CH, STR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2018-2024·2024-06-12
Vascular graft recalled due to swivel rod separation risk
Atrium Medical Corporation is recalling FLIXENE vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. The recall affects 53,308 units distributed worldwide.
Product
FLIXENE, 4-7X30, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1961-2024·2024-06-12
Vascular Graft Recalled Due to Slider Component Separation Risk
Atrium Medical's ADVANTA VXT vascular grafts are recalled due to reported separation of the slider component from the swivel core. Over 53,000 units worldwide may be affected.
Product
ADVANTA VXT, 8X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1941-2024·2024-06-12
Synchro2 Guidewires: PTFE coating damage from improper backloading technique
Stryker Neurovascular is recalling certain lots of Synchro2 Guidewires due to PTFE coating damage caused by backloading through an introducer accessory with manufacturing variations. Affected users should discontinue the backloading technique.
Product
The Synchro2 Guidewires are a steerable guidewire family with a shapeable tip and are available in straight and pre-shaped versions. The outside diameters of the guidewires are 0.014 in. The guidewires are compatible with existing microcatheters used in common procedures such as…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1302-2024·2024-06-12
Panera Kitchen Sink Cookie Recalled Due to Potential Salmonella Contamination
Panera Kitchen Sink Cookie dough pucks from Rise Baking Company are being recalled due to potential Salmonella contamination. The recall covers 29,019 cases distributed across 20 U.S. states.
Product
Panera Kitchen Sink Cookie, Net Wt. 45 lb (20.41 kg), 120/6 oz dough pucks/case
Category
Food
Distribution
21 states
HighFDA (Food)·F-1303-2024·2024-06-12
Rise Baking Company Cowboy Cookie recalled for potential Salmonella contamination
Rise Baking Company is recalling Cowboy Cookie dough pucks distributed across 20 states due to potential Salmonella contamination. Affected cases are identified by code 4117N1.
Product
Rise Baking Company Cowboy Cookie, Net Wt. 18.75 lb (8.5 kg), 300/ 1.0 oz dough pucks/case
Category
Food
Distribution
21 states
HighFDA (Devices)·Z-2014-2024·2024-06-12
Vascular graft component separation risk prompts medical device recall
Atrium Medical Corporation recalled FLIXENE vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. Over 53,000 units are affected worldwide.
Product
FLIXENE, 4-6X45, 2GDS, GWT. Double-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1295-2024·2024-06-12
Happy Farms Cream Cheese Spreads Recalled for Potential Salmonella
Happy Farms cream cheese spreads sold at Aldi were recalled due to potential Salmonella contamination affecting 835,721 units distributed across 19 states and Puerto Rico.
Product
Variety Tray Chive Onion (UPC 4099100 101751), Strawberry (UPC 4099100 101744), and Plain Cream Cheese Spread (UPC 4099100 101737), each container Net Wt. 8 oz. (226g). Keep Refrigerated, packaged under the brand Happy Farms, UPC . Dist & Sold Exclusively by Aldi, Batavia, IL…
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-1962-2024·2024-06-12
ADVANTA VXT Vascular Graft Slider Rod Separation Recall
Atrium Medical is recalling ADVANTA VXT vascular grafts due to reported separation of the slider rod from the swivel core, with a gap between components. Approximately 53,308 units are affected globally.
Product
ADVANTA VXT, 5X40, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2003-2024·2024-06-12
FLIXENE Vascular Graft Recall Due to Swivel Rod Component Separation
Atrium Medical recalls FLIXENE vascular grafts due to complaints of the Slider GDS Swivel Rod separating from the Swivel Core. Component separation in implanted vascular grafts could compromise device function.
Product
FLIXENE, 7X50, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1943-2024·2024-06-12
Arial Emergency Mobile App Restarts Cause Alert Overload and Call Failures
The Arial mobile application experiences frequent restarts on iOS 17.4 and 17.5, causing alert overload, communication failures, and offline status in healthcare facilities.
Product
Arial mobile application, model numbers 54640, 54630, and 54630-SMA, that utilizes Apple iOS 17.4 and Apple iOS 17.5, a component of the Arial Emergency and Nurse Call System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1987-2024·2024-06-12
Advanta VXT vascular grafts recalled for swivel rod separation
Atrium Medical Corporation is recalling the Advanta VXT vascular graft due to reports of the swivel rod separating from the swivel core. The recall affects approximately 53,308 units distributed in the United States and worldwide.
Product
ADVANTA VXT, 7X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1284-2024·2024-06-12
Charles Boggini Pink Lemonade Recalled for Undeclared Food Dye
Charles Boggini Pink Lemonade in 1 and 5-gallon sizes is recalled for containing undeclared FD&C Red No. 40. The colorant was not listed on product labels.
Product
Charles Boggini Pink Lemonde; 1 or 5 U.S. Gallons
Category
Food
Distribution
9 states
ModerateFDA (Devices)·Z-1947-2024·2024-06-12
Leica HistoCore PEGASUS tissue processor recalled for tissue damage
LEICA BIOSYSTEMS is recalling 141 Leica HistoCore PEGASUS tissue processors due to reagent overfilling that causes poorly processed or damaged biopsy tissue specimens.
Product
Leica HistoCore PEGASUS Tissue Processor, REF 14048858005.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0542-2024·2024-06-12
Estradiol Transdermal Patch Recalled for Failed Chemical Specifications
Zydus Pharmaceuticals is recalling Estradiol Transdermal System patches nationwide due to failed impurities and degradation specifications. The recall affects 21,360 units distributed throughout the United States.
Product
ESTRADIOL — ESTRADIOL (ESTRADIOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0541-2024·2024-06-12
Pregabalin Capsules Recalled Due to Foreign Tablet Contamination During Packaging
Rising Pharma's pregabalin capsules are being recalled nationwide after a pantoprazole tablet was discovered during packaging. No illnesses have been reported.
Product
PREGABALIN — PREGABALIN (PREGABALIN)
Category
Drug
Distribution
Distributed nationwide