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. 2,653 recalls have been distributed to New Jersey in the last 12 months.
Showing 25481–25500 of 29,496 recalls
Recalled Item: MicroScan Pos Combo Panel Type 33 (PC33): Catalog number B1017-211 Recalled...
The Issue: Siemens investigation confirmed that a portion one lot of panel Pos Combo 33...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intended for both adult and pediatric patients for taking diagnostic...
The Issue: In special cases, during the start-up of the current model of MobileDiagnost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes XRL Medium Trial - Central Body Recalled by Synthes, Inc. Due to Two...
The Issue: Two lots of the Synthes XRL Medium Trial-Central Body device were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Variant II beta-thalassemia Short Program Model Numbers 270-2103 (250 tests)...
The Issue: There is an issue with the buffers which impacts the quantification of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)...
The Issue: Separation events have occurred, including the VIPR separating from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SBi RingFix Olive Wires Product Usage: These are temporary devices Recalled...
The Issue: Small Bone Innovations (SBI) is recalling non-sterile RingFIX Olive Wires...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipase Reagent Recalled by Abbott Laboratories, Inc Due to Package inserts...
The Issue: Package inserts have incorrect SmartWash parameters for Triglyceride.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glucose Hexokinase Liquid Reagent For the in vitro quantitative...
The Issue: JAS Diagnostics, Inc. of Miami Lakes, FL is recalling their Glucose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit 8551/856X (includes Models 8561 Recalled by Medtronic Neuromodulation...
The Issue: Some kits in the affected lots may contain an extension tubing set that is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lithium Ion Battery M4605A and M4607A for use with IntelliVue Recalled by...
The Issue: The risk of battery failure increases with age, when a battery remains in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Imaging XS Syngo Imaging XS is a Picture Archiving Recalled by Siemens...
The Issue: A complaint reported that the archiving method at one customer site was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shimadzu Digital Radiography X-Ray System Recalled by Shimadzu Medical...
The Issue: Shimadzu Corporation is recalling the Shimadzu Digital X-Ray System because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...
The Issue: It has been identified that in a reject image workflow where multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprotte Spinal Tray / Sprotte Spinal Needle 24 gauge with Recalled by B....
The Issue: B.Braun Medical, Inc. (BBMI) has received reports of 24 gauge Sprotte...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medrad Continuum MR Infusion system- non-wireless system The MEDRAD...
The Issue: There is a potential safety risk associated with potentially damaged locking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Dynamics v9.5 system. A Picture Archiving and Communication System...
The Issue: Systems with the affected serial number are experiencing a software error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMIA v1.0 APD System. For Automated Peritoneal Dialysis (APD) therapy...
The Issue: Additional warning in the AMIA APD System labeling for patients vulnerable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iLab Ultrasound Imaging System Recalled by Boston Scientific Corporation Due...
The Issue: Specific iLab Ultrasound Imaging Systems using newest 3.0 (Polaris 1.0)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor with system software version...
The Issue: Software communication failure may occur on the HeartStart XL+ locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MDC PACS R2.X / IntelliSpace PACS DCX R3.1 software Recalled by...
The Issue: Philips MDC PACS Release R2.x and Philips IntelliSpace PACS DCX R3.x, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.