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. 1,083 recalls have been distributed to New Jersey in the last 12 months.
Showing 16781–16800 of 53,621 recalls
Recalled Item: 5Fr PowerPICC Catheter Single-Lumen with 70cm Guidewire Instructions For...
The Issue: Catheter kits contained the incorrect micro-introducers.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Recalled by...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 High Performance. radiography and fluoroscopy system...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90. radiography and fluoroscopy system Recalled by Philips...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Flex/Value/Chest/ER. radiography and fluoroscopy system...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 High Performance. radiography and fluoroscopy system...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex / Value. radiography and fluoroscopy system Recalled...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ADVIA Chemistry XPT Chemistry System Recalled by Siemens Healthcare...
The Issue: ADVIA Chemistry System and Software Versions (V1.4 SMN 11314625 and V1.4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortoss Bone Augmentation Material 5cc Cartridge Recalled by Stryker Spine...
The Issue: The products experienced a 12-hour excursion from the required temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortoss Bone Augmentation Material 10cc Cartridge Recalled by Stryker Spine...
The Issue: The products experienced a 12-hour excursion from the required temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PremierZEN Gold 7000 capsule Recalled by Miracle 8989 Due to Marketed...
The Issue: Marketed without an approved NDA/ANDA - Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: maXXzen Platinum 12000 capsule Recalled by Miracle 8989 Due to Marketed...
The Issue: Marketed without an approved NDA/ANDA - Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PremierZEN Platinum 8000 capsule Recalled by Miracle 8989 Due to Marketed...
The Issue: Marketed without an approved NDA/ANDA - Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Herniatome Recalled by ADRIA SRL Due to The recalling firm was notified by...
The Issue: The recalling firm was notified by the contract sterilizer that the process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Herniatome Recalled by ADRIA SRL Due to The recalling firm was notified by...
The Issue: The recalling firm was notified by the contract sterilizer that the process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JELCO HYPODERMIC NEEDLE-PRO FIXED NEEDLE INSULIN SYRINGE: a) 1.0mL 28G...
The Issue: Specific models and lot numbers of the Jelco Hypodermic Needle-Pro Fixed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Herniatome Recalled by ADRIA SRL Due to The recalling firm was notified by...
The Issue: The recalling firm was notified by the contract sterilizer that the process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clio Yogurt Bar Coconut Less Sugar Bar 45g x 10 Recalled by Clio LLC Due to...
The Issue: Possible metal fragments in Yogurt Bars
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clio Yogurt Bar Mixed Berry Low Sugar Bar 50g x Recalled by Clio LLC Due to...
The Issue: Possible metal fragments in Yogurt Bars
Recommended Action: Do not consume. Return to store for a refund or discard.