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. 2,674 recalls have been distributed to Delaware in the last 12 months.
Showing 4921–4940 of 27,373 recalls
Recalled Item: FilmArray Pneumonia Panel Plus (Pneumoplus) Recalled by BioFire Diagnostics,...
The Issue: Their is a potential for false positive results when using Pneumonia panel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Pneumonia Panel (Pneumo) Recalled by BioFire Diagnostics, LLC Due...
The Issue: Their is a potential for false positive results when using Pneumonia panel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT 7500: Software Version 5.0 Recalled by PHILIPS MEDICAL SYSTEMS...
The Issue: A software issue that can incorrectly label all captured images that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DiaSorin LIAISON HSV-2 Type Specific IgG Recalled by Diasorin Inc. Due to...
The Issue: DiaSorin has identified that lots 136344, 136344A, 136344B, 136344C, 136520,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Recalled by Maquet Cardiovascular, LLC Due to Express chest drains...
The Issue: Express chest drains are pre-packaged with sterile water syringes which have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT on Rails: Software Version 5.1.0.X Recalled by PHILIPS MEDICAL...
The Issue: A software issue that can incorrectly label all captured images that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Recalled by Maquet Cardiovascular, LLC Due to Express chest drains...
The Issue: Express chest drains are pre-packaged with sterile water syringes which have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE TUBE 4 ml FX Sodium Fluoride/Potassium Oxalate Recalled by Greiner...
The Issue: Tubes have missing additive/anticoagulant resulting in clotting in most...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Articulating Headrest Recalled by Steris Corporation Due to...
The Issue: Dual-articulating head rest may not stay in place or may fail to lock into...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion system Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: System may exhibit a loss of imaging functionality and data due to an issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Articulating Headrest Recalled by Steris Corporation Due to...
The Issue: Dual-articulating head rest may not stay in place or may fail to lock into...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Globus Medical Cranial Drill with Stop Recalled by Globus Medical, Inc. Due...
The Issue: Sterile-packed Cranial Drills may not be sterile due to a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus/Gyrus Paparrela-Type Vent Tube 1.02MM Recalled by Olympus...
The Issue: The expiration date is missing from the primary (inner) packaging. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-c Anesthesia System Recalled by Getinge Usa Sales Inc Due to Potential...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Globus Medical Cranial Drill Recalled by Globus Medical, Inc. Due to...
The Issue: Sterile-packed Cranial Drills may not be sterile due to a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-i C20 Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Globus Medical Cranial Drill with Stop Recalled by Globus Medical, Inc. Due...
The Issue: Sterile-packed Cranial Drills may not be sterile due to a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-e Anesthesia System Recalled by Getinge Usa Sales Inc Due to Potential...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-i C30 Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-i C40 Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.