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. 2,684 recalls have been distributed to New Jersey in the last 12 months.
Showing 20421–20440 of 29,496 recalls
Recalled Item: TP4 Kit with 10cc SafeSet Reservoir Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bifurcated SafeSet Kit with 03mL Flush Device Recalled by ICU Medical, Inc....
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Kit with SafeSet and 03mL Flush Device Recalled by ICU Medical, Inc....
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ PSA Assay Recalled by Siemens Healthcare Diagnostics, Inc Due...
The Issue: Communication provided to emphasize that the PSA values should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artoura Breast Tissue Expander 700 cc Product Usage: Tissue expanders...
The Issue: The CPX4 Tissue Expander may have been packaged in the Artoura Tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Distal Femoral Augment 75 X 5 RL/LM Product Usage: Recalled by...
The Issue: Contents of the package do not match the product labeling. Product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MENTOR 2" Tall Height TE With Sutures 450cc PN: 354-9313 Recalled by Mentor...
The Issue: Tissue expander product mix found: CPX4 350cc was placed in a carton for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Recon Targeting Arm Guide Recalled by Zimmer Biomet, Inc. Due to Old...
The Issue: Old revisions and new revisions of the soft tissue sleeve and recon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Recon Soft Tissue Sleeve Guide Recalled by Zimmer Biomet, Inc. Due...
The Issue: Old revisions and new revisions of the soft tissue sleeve and recon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPX4 Breast Tissue Expander 650 cc : Product Usage: Tissue Recalled by...
The Issue: The CPX4 Tissue Expander may have been packaged in the Artoura Tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MENTOR 2" Tall Height TE With Sutures 350cc PN: 354-9312 Recalled by Mentor...
The Issue: Tissue expander product mix found: CPX4 350cc was placed in a carton for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ddR Formula B X-ray System Recalled by Swissray Medical Due to Possible...
The Issue: Possible injury due to movement of the arm, calibration loss and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Module Model 8110 with software version 9.15 The Recalled by...
The Issue: A software anomaly with the Alaris Syringe module software version 9.15 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Line Catheterization Kit with Sharps Safety Features Permits access...
The Issue: Shipping carton labeling error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Calibrator U Recalled by Siemens Healthcare...
The Issue: Failure of analytical sensitivity with Calibrator U kit lots ending in 63...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features Permits access...
The Issue: Shipping carton labeling error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 23 G x .75 in. BD Vacutainer¿ Push Button Recalled by Becton Dickinson &...
The Issue: BD has received multiple reports of units associated with the 23 G x .75 in....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareLink iPro Version 1.10 Recalled by Medtronic Inc. Due to Medtronic...
The Issue: Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via picture archiving and communication system Syngo via is a Recalled...
The Issue: Software error. Incorrect values for the volume calculation from a freehand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e.cam and Symbia E gamma camera systems with patient beds Recalled by...
The Issue: "We have received reports of patients hair being caught in the e.cam and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.