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. 1,902 recalls have been distributed to Delaware in the last 12 months.
Showing 12961–12980 of 27,373 recalls
Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...
The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...
The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Body Weight Support (BWS) Light Recalled by MOTEK MEDICAL B.V. Due to The...
The Issue: The firm discovered a potential manufacturing deviation of the yoke of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...
The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...
The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...
The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Surgical System Recalled by Intuitive Surgical,...
The Issue: The firm become aware of a potentially defective capacitors on circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X Surgical System Surgical System Recalled by Intuitive Surgical,...
The Issue: The firm become aware of a potentially defective capacitors on circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe OmniBed Carestation CS1 - Product Usage: The device can Recalled by...
The Issue: Fasteners potentially torqued to a value less than the specified value and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci SP Surgical System Recalled by Intuitive Surgical, Inc. Due to The...
The Issue: The firm become aware of a potentially defective capacitors on circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endintrak 2 Hook Blade Recalled by Stryker GmbH Due to The seal integrity of...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Triangle Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Push Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrig ETF Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Triangle Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Triangle Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endintrak¿ 2 Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Hook Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.