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. 2,753 recalls have been distributed to New Jersey in the last 12 months.
Showing 15461–15480 of 29,496 recalls
Recalled Item: CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD) Recalled by DePuy...
The Issue: There is the potential for debris/material to be found behind the O-rings in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORAIL AMT HIGH OFFSET NECK SEGMENT (KHO) Recalled by DePuy Orthopaedics,...
The Issue: There is the potential for debris/material to be found behind the O-rings in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit Recalled by Arrow International Inc Due to...
The Issue: The products labeling contains inconsistencies. In certain instances, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StageOne Hip Recalled by Zimmer Biomet, Inc. Due to There is a potential for...
The Issue: There is a potential for comingling of the 43MM and 51 MM molds
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4.5 Recalled by RAYSEARCH LABORATORIES AB Due to Robust...
The Issue: Robust optimization for plans using beam set + background dose is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FocalPoint Slide Profiler and BD FocalPoint GS Review Station Recalled by...
The Issue: The device may not function at the lower end (<15 deg. C) of the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid IABP Recalled by Maquet Datascope Corp - Cardiac Assist...
The Issue: There is a potential for interruption and/or inability to start therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue IABP Recalled by Maquet Datascope Corp - Cardiac Assist...
The Issue: There is a potential for interruption and/or inability to start therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single-Use Biopsy Forceps Recalled by Micro-Tech (Nanjing) Co., Ltd. Due to...
The Issue: Single-Use Biopsy Forceps box contains incorrect product, instead it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AS-OBGYN Information System version 7.824.x Recalled by AS Software, Inc....
The Issue: Any change made to current ultrasound machine software or hardware upgrades,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost software 4.1.x and 4.2.x Recalled by Philips Medical...
The Issue: Stitching run on SkyPlate detector interrupted intermittently; Stitching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Access Cortisol Reagent. REF (Catalog Number) 33600 Recalled by Beckman...
The Issue: Cross contamination may have occurred between wells for the reagent pack. As...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 (PB980) ventilator series: Puritan Bennett" 980...
The Issue: Software Update: External USB Drive performance and its impact on Graphic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPECTRUM IQ INFUSION SYSTEM WITH DOSE IQ SAFETY SOFTWARE Recalled by Baxter...
The Issue: If an operator attempts to manually program a Basic Infusion for a drug that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Navigation 0-arm 02 Imaging System interventional fluoroscopic...
The Issue: O-arm 02 Imaging Systems correction to software version 4.1.0; new version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOND Slide Labeler Zebra Printer Model TLP3842 and Model GX4301 Recalled by...
The Issue: The power supply unit for the printer used with the device can potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NucliSENS¿ Magnetic Extraction Reagents Recalled by BioMerieux SA Due to...
The Issue: Data loggers showed that one shipment to the United States experienced low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Agilis Steerable Introducer: indicated for introducing various...
The Issue: Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE LOGIQ E10 Ultrasound System Recalled by GE Healthcare, LLC Due to There...
The Issue: There is a potential for an undetected over temperature condition on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Millennium MC Recalled by GE Healthcare, LLC Due to A detector...
The Issue: A detector can detach and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.