Product Recalls in New Jersey
Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,841 recalls have been distributed to New Jersey in the last 12 months.
Showing 5361–5380 of 53,621 recalls
Recalled Item: Wiers Farm - Spaghetti Squash packaged in 1lb cartons - Recalled by Wiers...
The Issue: Listeria monocyotgenes contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wiers Farm - Butternut Squash packaged in 1lb cartons - Recalled by Wiers...
The Issue: Listeria monocyotgenes contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Elin Dessert Plates. The recalled plates are lilac in color with orange...
The Issue: Elevated levels of cadmium in plates
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Healthy Living Acetaminophen Recalled by Aurobindo Pharma USA Inc Due to...
The Issue: Labeling: Missing Label - some bottles are missing the the manufacturers...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonazepam Orally Disintegrating Tablets Recalled by Endo Pharmaceuticals,...
The Issue: Labeling: Label Error on Declared Strength; Some cartons were incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer Recalled by Beckman...
The Issue: Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guidewire 70cm x 1mm (0.038 ) These accessories Recalled by Bard Peripheral...
The Issue: Due to guidewires being manufactured incorrectly with the guidewires being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Mishima...
The Issue: Due to a software issues, after the instrument processes 250 racks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Proton Therapy System - PROTEUS 235- Designed to produce Recalled by Ion...
The Issue: Temporary deactivation of collision detection for Forte Robotic Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VITROS XT Chemistry Products ALB-TP Slides is a single Recalled by...
The Issue: The reason for this recall is QuidelOrtho has determined that during normal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fox's u-bet Vanilla Flavored Syrup Recalled by SUBCO FOODS INC Due to...
The Issue: Customer complaint for bloated bottles. Testing and examination of these...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fox's u-bet Sugar-Free Chocolate Flavored Syrup Recalled by SUBCO FOODS INC...
The Issue: Customer complaint for bloated bottles. Testing and examination of these...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nitrofurantoin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic DLP Single Stage Venous Cannulae with right angle metal tip...
The Issue: During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BKIT BD Pyxis QFill Replenishment Station Recalled by CareFusion 303, Inc....
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis QFill Replenishment Station Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGrath Mac Video Laryngoscope Recalled by Covidien Due to Battery...
The Issue: Battery management system within Laryngoscope devices may deplete below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covideien McGRATH MAC Video Laryngoscope Recalled by Covidien Due to IFU...
The Issue: IFU update to address device's battery handling information.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGRATH" MAC EMS Video Laryngoscope Recalled by Covidien Due to Battery...
The Issue: Battery management system within Laryngoscope devices may deplete below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurora 4 Series Recalled by DKK Dai-Ichi Shomei Co., Ltd. Due to The weld on...
The Issue: The weld on the light head frame can crack which could lead to problems such...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.