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. 930 recalls have been distributed to Delaware in the last 12 months.
Showing 40501–40520 of 48,330 recalls
Recalled Item: Heparin Sodium in 5% Dextrose Injection Recalled by Hospira Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbidopa and Levodopa Tablets USP Recalled by Teva Pharmaceuticals USA Due...
The Issue: Failed Tablet/Capsule Specifications: Teva is recalling one lot of Carbidopa...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: APLENZIN¿ (bupropion hydrobromide) Recalled by Valeant Pharmaceuticals North...
The Issue: Labeling: Incorrect or Missing Package Insert
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: APLENZIN¿ (bupropion hydrobromide) Recalled by Valeant Pharmaceuticals North...
The Issue: Labeling: Incorrect or Missing Package Insert
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: APLENZIN¿ (bupropion hydrobromide) Recalled by Valeant Pharmaceuticals North...
The Issue: Labeling: Incorrect or Missing Package Insert
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Humidifier Adaptor 040 Recalled by Teleflex Medical Due to The seals of the...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adaptor Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis or Artis zee system Product Usage: Axiom Artis Recalled by...
The Issue: There is a potential problem with the AXIOM Artis or Artis zee system in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humidifier Adaptor Recalled by Teleflex Medical Due to The seals of the...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 101 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excelsior Medical Sterile Triple Lead Tubing Set and Sterile Heavy Recalled...
The Issue: There is a potential for a leak. A molding defect in the connector that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraStream Peel Away Kit Recalled by Argon Medical Devices, Inc Due to...
The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak SW/EAU Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraStream Exchange Kit Model Numbers 32001524 (24 cm) Recalled by Argon...
The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.