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. 997 recalls have been distributed to Delaware in the last 12 months.
Showing 21781–21800 of 48,330 recalls
Recalled Item: BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number:...
The Issue: Lot has been confirmed to have no additive within the tube. Sample processed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-fog solution packaged in a Tyvek peel pouch and it Recalled by Medline...
The Issue: The Anti-Fog Solution may not defog properly due to a degradation in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liberty Cycler Cassettes (a disposable cassette that is intended to Recalled...
The Issue: Additional Instructions: step-by step handling and inserting the cassette...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SLIM Handle - catalogue #: SLM-HND100 a component of Simple Recalled by Pega...
The Issue: Handle could jam with the Driver due to the detachment of an internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPi-Sense Guided Coagulation System with Visitrax Recalled by AtriCure, Inc....
The Issue: The sterile package seal for the Epi-Sense Guided Coagulation System may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stratus CS Acute Care cTNI TestPak Recalled by Siemens Healthcare...
The Issue: Potential for increased rate of false positive results and/or increased rate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.All (Model #11061630) Recalled by Siemens Medical Solutions USA,...
The Issue: The potential sporadic performance problems may result in scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811901 Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811910...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229034A Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229035A...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811911 Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Top (Model #1161640) Recalled by Siemens Medical Solutions USA,...
The Issue: The potential sporadic performance problems may result in scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Now (Model #11061620) Recalled by Siemens Medical Solutions USA,...
The Issue: The potential sporadic performance problems may result in scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 10 Fr 3 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 6 Fr 1.5 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 8 Fr 3 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229036A...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.