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. 1,785 recalls have been distributed to Delaware in the last 12 months.
Showing 29581–29600 of 48,330 recalls
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: If Hip Recalled by Breg Inc Due to They may not have been sealed prior to...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport Medical HT70 and HT70- Plus Ventilators Recalled by Newport Medical...
The Issue: Medtronic is issuing a voluntary field corrective action for all its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18L6 HD transducer on the ACUSON S Family ultrasound systems Recalled by...
The Issue: When scanning with the 18L6 HD transducer on the ACUSON HELX" Evolution with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Therm Hyper/Hypothermia System Recalled by Stryker Medical Division of...
The Issue: The water may reheat too quickly if the unit is in "Automatic" mode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LaBri's Body Health Atomic Recalled by Envy Me Due to Undeclared Sibutramine
The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared Sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PrednisoLONE Oral Solution USP Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: hCG Body Shaper Recalled by Gary Wood Due to Marketed without an Approved...
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis has found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin and Triamcinolone Acetonide Cream Recalled by Taro Pharmaceuticals...
The Issue: Failed Content Uniformity Specifications; out-of-specification (OOS) results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE426R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...
The Issue: Diamond particulates may break off the burr and fall into the surgical site....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GP321R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...
The Issue: Diamond particulates may break off the burr and fall into the surgical site....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GP161R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...
The Issue: Diamond particulates may break off the burr and fall into the surgical site....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR GHIATAS Beaded Breast Localization Wire Recalled by Bard Peripheral...
The Issue: It may be at risk of containing a non-MR compatible GHIATAS Beaded Breast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delta Recalled by Draegar Medical Systems, Inc. Due to It was reported that...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delta XL Recalled by Draegar Medical Systems, Inc. Due to It was reported...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kappa Recalled by Draegar Medical Systems, Inc. Due to It was reported that...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Patient Care Kits Product Usage: A Patient Care Kit Recalled by Alcon...
The Issue: Alcon is initiating a Voluntary Medical Device Removal because the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.