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. 2,620 recalls have been distributed to Delaware in the last 12 months.
Showing 13321–13340 of 27,373 recalls
Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...
The Issue: The action is being initiated due to complaints received concerning the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REVACLEAR 400 Dialyzer Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential presence of ruptured dialyzer fibers which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEO Patient Monitor /Tranquility VS Patient Monitor Recalled by Infinium...
The Issue: The CLEO & Tranquility VS Patient Monitors 510(k) indications for use in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REVACLEAR 300 Dialyzer Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential presence of ruptured dialyzer fibers which may lead to...
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: 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: 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: 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: 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: 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: 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: 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: 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.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: ARDVST229003A 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: ARDVST229000A 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: ARD568812910 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.