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All product recalls affecting New Jersey.
Includes nationwide recalls (tagged “Nationwide”) and recalls with New Jersey in the distribution area.
This recall involves certain Cabinet Health 4 oz. Refillable Medicine Bottles with ABS plastic lids. The bottles are made of clear glass with blue, turquoise, orange or purple plastic lids labeled \"CABINET.\" Cabinet Health sold the bottles filled with over-the-counter drugs or as empty 4 oz. bottles. The recalled empty 4 oz. bottles were sold via cabinethealth.com from March 2023 through July 2024. Consumers with recalled empty bottles can identify them by the date of purchase. The recalled bottles filled with over-the-counter drugs have the following date codes on a sticker on the bottom of the bottle. Medication Name Lid Color Date Codes Tension Headache - Refillable Glass Bottle (Acetaminophen 500mg Caffeine 65mg) - 100 Count Blue 2029J07223 2029J07623 2029J07723 Allergy Relief - Refillable Glass Bottle (Diphenhydramine HCl 25mg) - 120 Count Turquoise 2265J07323 Pain Reliever and Nighttime Sleep Aid - Refillable Glass Bottle (Acetaminophen 500mg, Diphenhydramine 25mg) - 120 Count Blue 2127J06823 2127J23323 3040J23323 3051J23323 3051J23423Pain Reliever and Fever Reducer - Refillable Glass Bottle (Acetaminophen 500mg) - 120 Count Blue 2286J06323 2286J06523 2286J06623 2287J06623 2287J06723 Cough Relief - Refillable Glass Bottle (Dextromethorphan Hbr 15mg) - 60 Count Orange 2010J06923 2010J07023 3004J29623 3010J29623 3025J29623 Sleep Aid - Refillable Glass Bottle (Diphenhydramine HCl 50mg) - 70 Count Purple 3021J06823 3021J06923 3034J23423 3034J23523
This recall involves three multipack hair dryer bundles. The three bundles were sold in either light gray or light green colors. The 6-in-1 Multi Styler hair dryers have more than three heating modes, with model number HS01 on the underside of the product. They are powered by the V9 digital motor and measure approximately 16 inches (length) x 7 inches (width) x 5 inches (height) and weigh four pounds. The 5-in-1 Multi Styler hair dryers have more than three heating modes, with a model number HS01 on the underside of the product. They are powered by the V9 digital motor and measure approximately 14 inches (length) x 6 inches (width) x 4 inches (height) and weigh four pounds.
This recall involves the AMX Global Portable Folding Stadium Seat sold under the BJ's Wholesale or Black Sierra brand. The BJ's units have the "Berkley Jensen" logo on the back top side. The Black Sierra units have a Black Sierra Equipment logo on the top, right front side. The stadium seats fold down to a compact size of about 4 inches by 20 inches by 19 inches from the open size of 16 inches by 20 inches by 19 inches. They have a padded handle and shoulder strap. Recalled Berkley Jensen seats have the date code "04/2022" on the white tag on the bottom of the seat. Recalled Black Sierra Equipment seats have the date codes "05/2022" or "11/2022" on the white tag on the bottom of the seat. Only those date codes are included in this recall.
This recall involves Greater Goods Digital Kitchen Scales, models: 0480, 0455, 0456, 0458, 0473, 0479, 0481, 0747, 0748, 0749, 0751, 0752, 0754. They are labeled with a sticker with the brand and model printed on the back and come in gray, black, blue, green, pink, red, silver and white colors. The Greater Goods logo is located on the top of the front panel of the scale. The scales come with a lithium CR3032 coin battery pre-installed and a spare CR3032 battery in the packaging.
Failed Dissolution Specifications.
Autocar, LLC (Autocar) is recalling certain 2024-2025 ACX (Xpeditor) vehicles. A software error may cause the forward collision sensing radar to fail.
Firm became aware of software issues related to most recent firmware update which could result in loss of patient tissue.
Autocar, LLC (Autocar) is recalling certain 2023 Autocar DC (Legend) trucks. The forward collision warning (FCW) system may be inoperative due to a software error.
Increase in complaints concerning "pullwire" breakage that may result in the broken pullwire remaining in the anchor implant body after deployment.
During endoscopic procedures using a combination of the video processor EPK-i8020c and the i20c series video endoscope, the observed image can become reddish or dark (1.8%). Users have observed smoke-like steam and noted that the light guide at the tip is hot during use / after the endoscope is removed from the patient, and may cause thermal injury to the patient's mucous membranes.
During endoscopic procedures using a combination of the video processor EPK-i8020c and the i20c series video endoscope, the observed image can become reddish or dark (1.8%). Users have observed smoke-like steam and noted that the light guide at the tip is hot during use / after the endoscope is removed from the patient, and may cause thermal injury to the patient's mucous membranes.
During endoscopic procedures using a combination of the video processor EPK-i8020c and the i20c series video endoscope, the observed image can become reddish or dark (1.8%). Users have observed smoke-like steam and noted that the light guide at the tip is hot during use / after the endoscope is removed from the patient, and may cause thermal injury to the patient's mucous membranes.
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2023 Toyota Corolla, Corolla Cross, Corolla Cross Hybrid, Highlander, Highlander Hybrid, Tacoma, Lexus RX350, 2023-2024 NX250, and NX350 vehicles that may have been incorrectly repaired under previous NHTSA recall number 23V-480. An electrical connection inside the steering column's spiral cable assembly may be insufficiently welded, causing the connection to separate and deactivate the driver's air bag. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 208, "Occupant Crash Protection."
PACCAR Incorporated (PACCAR) is recalling certain 2025 Kenworth T180, Peterbilt 535, 567, 2025-2026 Kenworth T280, 2023-2026 Kenworth T380, 2024-2026 Kenworth T480, 2024-2026 Peterbilt 536, 537, and 548 trucks. The exterior lighting switch may fail, resulting in the hazard lights and the instrument display back-light brightness adjustment not functioning. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) numbers 101, "Control and Displays" and 108, "Lamps, Reflective Devices and Associated Equipment."
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.
CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit.