Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,678 recalls have been distributed to Delaware in the last 12 months.
Showing 4001–4020 of 27,373 recalls
Recalled Item: Ingenia 1.5T S Model Number (REF): 781347 Recalled by Philips North America...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AchievaXR -Magnetic Resonance (MR) systems are Medical Electrical Systems...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T TX for PET Model Number (REF): 781479 Recalled by Philips North...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX - Magnetic Resonance (MR) systems are Medical Recalled by...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis: MedStation ES (Main) Recalled by CareFusion 303, Inc. Due to If...
The Issue: If automated dispensing cabinets have specific software versions, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Interventional Hemodynamic Application R.1.2X Recalled by PHILIPS...
The Issue: Potential for pressure wave data synchronization from two devices may not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The D*Clot¿ HD Rotational Thrombectomy System is a percutaneous...
The Issue: Internal product testing failed bubble leak testing (ASTM F2096), which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL 731 Ventilator (EMV+ Recalled by ZOLL Medical Corporation Due to...
The Issue: Operator's Guide & Quick Guide (QRG) ZOLL 731 Ventilator for MRI Compatible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TabloCart with Prefiltration Drawer PN-0006813 Recalled by Outset Medical,...
The Issue: A cart with prefiltration drawer, an optional hemodialysis system accessory,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE STERILE IRIS SCISSORS CVD/STD (case) and DYNJ04049H Recalled by...
The Issue: There is the potential of the tip protector to fall off 4.5" sterile,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BSM-3000 Series Bedside Monitor The Life Scope BSM-3000 Recalled by Nihon...
The Issue: Due to software issue the device may give false "SpO2 Probe Failure" alarm
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FiberOptix Intra-Aortic Balloon Catheter Kit: a) Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow UltraFlex Intra-Aortic Balloon Catheter Kit Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Ultra 8 IAB Intra-Aortic Balloon Catheter Kit Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDC Recalled by Centers For Disease Control and Prevention Due to The H5b...
The Issue: The H5b component may fail to amplify, resulting in an inconclusive result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm O2 Imaging System-Mobile x-ray system designed for 2D fluoroscopic...
The Issue: Potential for an electrical component of the O-arm" O2 Imaging System to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EsoFLIP Recalled by Covidien, LLC Due to Due to saline conductivity issues,...
The Issue: Due to saline conductivity issues, their is a potential that dilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STARDRIVE SCRWDRVR SHFT/T4 50MM/SELF-RETAINING/HXC-Intended for tightening...
The Issue: Stardrive Screwdrivers manufactured without a 5-degree relief cut around the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasySuite 4K Integrated Operating Room System Model/Catalog Number:...
The Issue: A subset of the ES4K systems do not have complete records for earth leakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EsophaCap Product Name: EsophaCap (25mm diameter Recalled by...
The Issue: The EsophaCap sponge may be at increased risk of detaching from the string...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.