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. 2,595 recalls have been distributed to Delaware in the last 12 months.
Showing 13941–13960 of 27,373 recalls
Recalled Item: Covidien Endo Grasp Auto Suture Grasper 5mm The Recalled by COVIDIEN LLC Due...
The Issue: Sterilization method used was not consistent with the labeling and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure kits include devices from the affected lots distributed OUS...
The Issue: Sterilization method used was not consistent with the labeling and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truliant Tibial Fit Tray Cemented SZ 3F / 3T Recalled by Exactech, Inc. Due...
The Issue: 2.5 Truliant Fit Trays were mismarked as 3
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS II SUTURE 18"(45CM) 2-0 VIO Product Code:Z739D - PDS Recalled by...
The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICRYL PLUS Sutures: VICRYL PLUS SUTURE 18"(45CM) 3-0 VIO VICRYL Recalled by...
The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICRYL Sutures VICRYL SUTURE 18"(45CM) 0 VIO VICRYL SUTURE 18"(45CM)...
The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Unity Recalled by Elekta Limited Due to Users need to be aware when...
The Issue: Users need to be aware when using these protocols for daily on line plan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beaver Xstar Slit Knife 2.4 mm Recalled by Beaver Visitec Due to Mislabeling
The Issue: Mislabeled. The package labeling indicates a size 2.4mm, 45 degree Double...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Cardiac Control Recalled by Randox Laboratories Ltd. Due to Customers...
The Issue: Customers may observe a decrease in recovered concentration with regards to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics Due...
The Issue: One of the software algorithms used to detect sample dispense errors was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RT Elements Software revisions of the RT Elements applications have Recalled...
The Issue: There is a potential for an incorrect dose distribution calculation by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades:Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Blades Monopolar Recalled by Gyrus ACMI, Inc. Due to Olympus...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Malleable Recalled by Gyrus ACMI, Inc. Due to Olympus Diego...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.