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. 2,661 recalls have been distributed to Delaware in the last 12 months.
Showing 6781–6800 of 27,373 recalls
Recalled Item: Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution Recalled by...
The Issue: MiniCap Disconnect Cap with Povidone-Iodine are packaged in foil pouches,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fusion Bioline Vascular Graft Recalled by Maquet Cardiovascular, LLC Due to...
The Issue: One (1) Fusion Bioline Vascular graft from lot 25162546, which failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Tacrolimus (TAC) Flex reagent cartridge-In vitro diagnostic test...
The Issue: Siemens Healthineers has received customer complaints and confirmed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa COVID-19 Direct Recalled by DiaSorin Molecular LLC Due to Direct...
The Issue: Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD5 Series of Genesis Reusable Rigid Sterilization Container Systems catalog...
The Issue: Product did not meet shelf-life testing requirements resulting in a breach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Flu A/B & RSV Direct Gen II Recalled by DiaSorin Molecular LLC Due...
The Issue: Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For...
The Issue: After pressing and releasing the Z-Axis Motorized buttons on the Tube Head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Triglycerides (concentrated)-In vitro diagnostic use in the...
The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH LDL Cholesterol Direct (DLDL)-In vitro diagnostic quantitative...
The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Total Protein II- In vitro diagnostic use in Recalled by Siemens...
The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Triglycerides_2: in vitro diagnostic use in the quantitative...
The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Immunoassay Systems (1) Access 2 Immunoassay Analyzer (81600N)...
The Issue: An increased incidence of damage to the nut band from a new vendor (Boamax)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)...
The Issue: Manufactured with misaligned axis resulting in lenses with the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biofinity XR Toric Single Diagnostic lens- Soft (hydrophilic) Contact Lens...
The Issue: Manufactured with misaligned axis resulting in lenses with the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Easy Read App associated with First Response Pregnancy Test Sticks Recalled...
The Issue: Church & Dwight First Response Pregnancy Kits was marketed with the Easy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Black Intelligent Reload Recalled by Covidien, LP Due to...
The Issue: Affected lots have the potential for a broken sled vane, which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triton Canister Software Catalog Number: GAUS-2. Intended adjunct in the...
The Issue: Triton Canister Software, Insert & Scanning Label may cause the Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life2000 Ventilator PKG Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is the potential for patient desaturation events to occur under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Finished Goods Box of 50 Inserts and Scanning Labels for Recalled by Stryker...
The Issue: Triton Canister Software, Insert & Scanning Label may cause the Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life2000 Ventilator PKG Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is the potential for patient desaturation events to occur under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.