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 14001–14020 of 27,373 recalls
Recalled Item: SetSource ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical Oncology Kit w/12" (30cm) Ext Set w/Spiros w/Red Cap Recalled by...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical ChemoLock Recalled by ICU Medical, Inc. Due to There is a...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical Oncology Kit w/12" Ext Set w/Spiros w/Red Cap Recalled by ICU...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Synapsys Laboratory Solutions Catalog Number:444150 Product Usage: BD...
The Issue: BD Synapsys version 2.1 allowed the potential for a test order to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 3600 Immunoassay System-Software V3.3.2 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ ECi/ECiQ Immunodiagnostic System Product Code: 1922814 For use in...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 5600 Integrated System -Software V3.3.2 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 5600 Integrated System V3.3.2 & below Product Code: Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS ECi Immunodiagnostic System Product Code: 6801059 For use Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ XT 7600 Integrated System-Software V3.4.1 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 3600 Immunoassay System V3.3.2 & below Product Code: Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELL-DYN Emerald analyzer Recalled by Abbott Laboratories Due to There is a...
The Issue: There is a potential for the device to generate Quality Control (QC) low or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilite C-Reactive Protein Kit - Product Usage: The Optilite C-Reactive...
The Issue: Deterioration of C-reactive protein (CRP) reagent in Optilite C-Reactive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector...
The Issue: Additional units have been identified for previous recall Z-1280-2016 (RES...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Switches used with the following systems: 722001 Allura Xper Recalled...
The Issue: Additional units have been identified for previous recall Z-1280-2016 (RES...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro Knife 5.0mm 30¿ Recalled by Beaver Visitec Due to The product contains...
The Issue: The product contains a misprinted expiration date on the peel pack. Both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 8mm intended to Recalled by Avitus...
The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.