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 12421–12440 of 27,373 recalls
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook Safety Infusion System Y-type Blood Set Recalled by B. Braun...
The Issue: Potential for leakage at the joint between the blood filters and tubing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EVO Ventilator Recalled by Philips Respironics, Inc. Due to Software...
The Issue: Software defect in the Trilogy EVO and Trilogy EVO Universal Ventilator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EVO Ventilator Recalled by Philips Respironics, Inc. Due to Software...
The Issue: Software defect in the Trilogy EVO and Trilogy EVO Universal Ventilator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EVO Ventilator Recalled by Philips Respironics, Inc. Due to Software...
The Issue: Software defect in the Trilogy EVO and Trilogy EVO Universal Ventilator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EVO Ventilator Recalled by Philips Respironics, Inc. Due to Software...
The Issue: Software defect in the Trilogy EVO and Trilogy EVO Universal Ventilator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry CardioPhase High Sensitivity C-Reactive Protein (hsCRP)...
The Issue: Atellica and ADVIA hsCRP calibrator accuracy has drifted away from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Garbin EVO Ventilator Recalled by Philips Respironics, Inc. Due to Software...
The Issue: Software defect in the Trilogy EVO and Trilogy EVO Universal Ventilator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH High Sensitivity C-Reactive Protein (HsCRP) Calibrator - Product...
The Issue: Atellica CH: The Atellica¿ CH High Sensitivity CReactive Protein Calibrator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeVent EVO Ventilator Recalled by Philips Respironics, Inc. Due to...
The Issue: Software defect in the Trilogy EVO and Trilogy EVO Universal Ventilator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EVO Ventilator Recalled by Philips Respironics, Inc. Due to Software...
The Issue: Software defect in the Trilogy EVO and Trilogy EVO Universal Ventilator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EVO Ventilator Recalled by Philips Respironics, Inc. Due to Software...
The Issue: Software defect in the Trilogy EVO and Trilogy EVO Universal Ventilator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EVO Ventilator Recalled by Philips Respironics, Inc. Due to Software...
The Issue: Software defect in the Trilogy EVO and Trilogy EVO Universal Ventilator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EVO Ventilator Recalled by Philips Respironics, Inc. Due to Software...
The Issue: Software defect in the Trilogy EVO and Trilogy EVO Universal Ventilator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EVO Ventilator Recalled by Philips Respironics, Inc. Due to Software...
The Issue: Software defect in the Trilogy EVO and Trilogy EVO Universal Ventilator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.