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. 2,642 recalls have been distributed to New Jersey in the last 12 months.
Showing 26901–26920 of 29,496 recalls
Recalled Item: MHI-TM2000 Linear Accelerator System Recalled by MITSUBISHI HEAVY...
The Issue: Software anomaly: Mitsubishi Heavy Industries, Ltd. became aware of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Picis ED Pulsecheck - EMR Software Application - 2125 Recalled by Picis Inc....
The Issue: Notes associated with prescription are not printed to the prescription or to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-2.5 mL LeGoo with 1 Cannula Pouch Recalled...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo Internal Vessel Occluder 1mL Product Number: 10-0100 LeGoo is Recalled...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo Endovascular Occlusion Gel 2.5 mL Product Number: LG250IT LeGoo...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo Endovascular Occlusion Gel 1.0 mL Product Number: LG100IT LeGoo...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel- 1.0 mL LeGoo w/ no Cannula Recalled by...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo Endovascular Occlusion Gel 0.5 mL Product Number: LG50IT LeGoo...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel- 0.5 mL LeGoo with 3 Cannula Recalled by...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo Internal Vessel Occluder 5mL Product Number: 10-0500 LeGoo is Recalled...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-1.0 mL LeGoo with 3 Cannula Pouch Recalled...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo Internal Vessel Occluder 10mL Product Number: 10-1000 LeGoo is...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo Internal Vessel Occluder 2.5mL Product Number: 10-0250 LeGoo is...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo Internal Vessel Occluder .25mL Product Number: 10-0025 LeGoo is...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.5 mL LeGoo w/ no Cannula Product...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TEG 5000 Thromboelastograph Coagulation Analyzer Product Usage: Multipurpose...
The Issue: Research Use Only (RUO) parameters were included in TEG 5000 User Manual.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX Revolution Recalled by Carestream Health Inc. Due to Carestream Health...
The Issue: Carestream Health Inc. is conducting a recall for the Column end Cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Free Lock Femoral Hip Fixation System Compression Tube/Plate Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Free Lock Femoral Hip Fixation System Compression Lag Screw . Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.