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 16181–16200 of 29,496 recalls
Recalled Item: DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Release 3 (Stitching Patient Support) 712025 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips Medical Systems Gmbh, DMC Due to...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4.1 (Stitching Patient Support) 712225 Recalled by Philips...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Release 3 (Stitching Patient Support) 712025 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Upgrades (Stitching Patient Support) 712083 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4.1 Chest / Emergency (Stitching Patient Support) 712029...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Recalled by Philips Medical Systems Gmbh, DMC Due to The...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: Recalled by...
The Issue: Genicon is providing updated IFU labeling to users to provide clarity on how...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monitor with one Blood Parameter Module and one HSat Probe Recalled by...
The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrument trays used to store AltiVate Small Shell Trials (FA Recalled by...
The Issue: A black, aluminum oxide coating may appear on the tray after cleaning. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood parameter monitoring system 500 H/SAT Recalled by Terumo...
The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica M530 OHX Microscope System Supplied with 100 - 120 Vac. Recalled by...
The Issue: Recall is due to a design weakness of the power insert module.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT CLEARVUE isp Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: Certain NAUTILUS DELTA Port Kit product code / lot number combinations may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This is an accessory to Intelect Advanced Recalled by DJO, LLC Due to The...
The Issue: The device accessories were not labeled with appropriate latex warning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno Model 10849000. Interventional Fluoroscopic X-Ray System Product...
The Issue: Potential hardware issue which may cause thermal effects and possible damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.