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. 2,874 recalls have been distributed to New Jersey in the last 12 months.
Showing 1181–1200 of 29,496 recalls
Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...
The Issue: Their is the potential for weak staining which may result in false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...
The Issue: Their is the potential for weak staining which may result in false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...
The Issue: Their is the potential for weak staining which may result in false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP). Material Number:...
The Issue: Potential for falsely depressed patient, quality control (QC), and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Hemo Recalled by Merge Healthcare, Inc. Due to Merge Healthcare has...
The Issue: Merge Healthcare has been informed by Schiller AG (Baar, Switzerland) of an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2% Recalled...
The Issue: Blood collection tubes were manufactured with the label applied too high on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Medline Convenience Kits: 1) MAJOR PACK L-F Recalled by Medline...
The Issue: Convenience kits labeled as sterile have not gone through the sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argus PB-3000 Recalled by Schiller, Ag Due to Vital sign monitoring...
The Issue: Vital sign monitoring instrument may trigger an error message during blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Medline Convenience Kits: 1) EXTREMITY PACK Recalled by Medline...
The Issue: Convenience kits labeled as sterile have not gone through the sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baster Continu-Flo Solution Set Recalled by Baxter Healthcare Corporation...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Cardiovascular Recalled by Philips Medical Systems Nederland...
The Issue: Software issue that results in the display of outdated information.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 11B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 8B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 11A...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 9B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 6 Service...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 10B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 12A...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 7 Recalled...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 2023B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.