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. 2,020 recalls have been distributed to Delaware in the last 12 months.
Showing 2761–2780 of 27,373 recalls
Recalled Item: Garbin Evo. Model Number: LD2110X23B. Intended for invasive and non-invasive...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeVent EVO2. Model Number: SP2100X26B. Intended for invasive and...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2. Model Numbers: FP2100X10 Recalled by Philips Respironics,...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EV300. Model Numbers: DS2200X11B Recalled by Philips Respironics,...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Zenition 50 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Potential for the Mains Control Unit board fuse may blow out during system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Patient...
The Issue: As a result of a cloud data migration of Patient and Hospital Electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Hosptial...
The Issue: As a result of a cloud data migration of Patient and Hospital Electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...
The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Rocker-Switch...
The Issue: There is a potential for the product to activate without manual input when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTHROSCOPY Convenience kit used for surgical procedures Recalled by MEDLINE...
The Issue: Products within a Medline pack may be impacted by a packaging error in which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...
The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Push-Button Recalled...
The Issue: There is a potential for the product to activate without manual input when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...
The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....
The Issue: Potential failure of affected units to recharge the battery of the oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...
The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...
The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...
The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...
The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....
The Issue: Potential failure of affected units to recharge the battery of the oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.