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. 2,623 recalls have been distributed to Delaware in the last 12 months.
Showing 12701–12720 of 27,373 recalls
Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 45mm Needle+Stabilizer Kit...
The Issue: The safety cap attached to needles within the needle sets may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 15mm Needle+Stabilizer Kit...
The Issue: The safety cap attached to needles within the needle sets may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxymetry Cable Recalled by Edwards Lifesciences, LLC Due to Intermittent...
The Issue: Intermittent communication due to inconsistent crimping of connectors onto...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Legacy 3 Implant Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Some dental implant packages contain incorrect implants, which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH Slidemaker Stainer (DxH SMS) and UniCel DxH Slidemaker Recalled...
The Issue: When the UniCel DxH Slidemaker Stainer and UniCel DxH Slidemaker Stainer II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software versions syngo CT VB20 running on the following Siemens Recalled by...
The Issue: Software issue identified in the software versions syngo CT VB20 running on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAG SCREW 3.2MM GUIDE PIN SLEEVE Recalled by Smith & Nephew, Inc. Due to LAG...
The Issue: LAG SCREW 3.2 GUIDE PIN SLEEVE are being recalled due to a manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number: 06917259001 UDI: 04015630976010 - Product Usage: The System...
The Issue: The firm became aware of a cleaning solution leaking issue from the middle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Homocysteine-In vitro test for the quantitative determination of total...
The Issue: Homocysteine Reagent, Calibration Failures and Quality Control Recovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Liquid Cardiac Controls Catalogue Numbers CQ5053. Recalled by Randox...
The Issue: Removal of claims for N-proBNP in the Liquid Cardiac Control catalogue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK Hem-O-Lok AutoEndo5 Recalled by Teleflex Medical Due to Certain clip...
The Issue: Certain clip appliers have an increase in misloading and/or jamming related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK AutoEndo5 Recalled by Teleflex Medical Due to Certain clip appliers...
The Issue: Certain clip appliers have an increase in misloading and/or jamming related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Liquid Cardiac Controls Catalogue Number CQ5051 Recalled by Randox...
The Issue: Removal of claims for N-proBNP in the Liquid Cardiac Control model numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Liquid Cardiac Controls Catalogue Number CQ5052. Recalled by Randox...
The Issue: Removal of claims for N-proBNP in the Liquid Cardiac Control catalogue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neocis Guidance System Fiducial Array - Product Usage: The Neocis Recalled...
The Issue: The Fiducial Array may mismatch their measurement files resulting in failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.