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. 1,120 recalls have been distributed to New Jersey in the last 12 months.
Showing 12041–12060 of 53,621 recalls
Recalled Item: Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000...
The Issue: Warehouse experienced temperature excursions in July and August 2021. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg Recalled by SUN...
The Issue: Presence of Foreign Substance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Susvimo (ranibizumab injection) Recalled by Genentech Inc Due to Defective...
The Issue: Defective Delivery System: Commercial implants do not meet the filed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GFUEL brand Watermelon Limeade Energy Drink Recalled by G FUEL LLC Due to...
The Issue: Product label does not declare the correct amount of caffeine.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GI4000 Electrosurgical Unit - intended to deliver electrosurgical outputs to...
The Issue: Two electronic diode components (D1 & D4) placed in the reverse orientation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerate PhenoTest BC kit Recalled by Accelerate Diagnostics Inc Due to...
The Issue: Due improperly formulated and released bulk lot of fluorescence in situ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerate PhenoTest BC kit Recalled by Accelerate Diagnostics Inc Due to...
The Issue: Due improperly formulated and released bulk lot of fluorescence in situ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18239: ASM Omnipod Dash PDM Recalled by Insulet Corporation Due to The firm...
The Issue: The firm has become aware of PDM battery issues, including battery swelling,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope...
The Issue: Broken Optical fiber cable damage can occur through handling or bending and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam...
The Issue: Broken Optical fiber cable damage can occur through handling or bending and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium - Visionsense Infrared (IR) Fluorescence Miniature Microscope...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Laser System Recalled by Spectranetics Corporation Due to Laser...
The Issue: Laser System may detect Error 106 or Error 108 System Failures that will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE FIBER...
The Issue: Due to a defect in the outer pouch sterile seal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GentleWave System APM Procedure Instrument with Matrix Recalled by Sonendo...
The Issue: Procedure Instruments with erroneous unit carton labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GentleWave System Posterior CleanFlow Procedure Instrument with Matrices...
The Issue: Procedure Instruments with erroneous unit carton labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extension Tabletop for Operating Table System 1140 Recalled by Getinge Usa...
The Issue: The back rest may unintentionally drop suddenly, resulting in adverse health...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-107: The Phoenix PMIC/ID panel is used for Recalled by...
The Issue: Misformulated minocycline-can cause erroneously increased Minimal Inhibitory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 9 -(GEN) 22 of VITROS Recalled by...
The Issue: Calibration disk Data Release Version (DRV) 6194 to 6200 contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hammond's Salted Caramel Cookies Recalled by Hammond's Candies Since 1920...
The Issue: Peanut Butter Chocolate Chip Cookies mispacked in Salted Caramel Cookies Box...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Artificial Tears OINTMENT Recalled by Akorn, Inc. Due to CGMP Deviations:
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.