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. 2,623 recalls have been distributed to Delaware in the last 12 months.
Showing 12881–12900 of 27,373 recalls
Recalled Item: Remisol Advance running on hardware with Windows XP Recalled by Normand-Info...
The Issue: A patch was released for a critical remote code execution vulnerability in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9646 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9653 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9632 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9627 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9615 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Issues Scanning New Reagent Lot Test Definition on the Atellica IM 1300...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Issues Scanning New Reagent Lot Test Definition on the Atellica IM 1300...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquilex Fluid Control System component: Bag deflector Recalled by WOM World...
The Issue: The deficit displayed by the pump can differ from the real deficit, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM anti-CCP IgG (aCCP) Assay Siemens Material Number: 10732998...
The Issue: Atellica IM anti-CCP IgG (aCCP) Test Definition (TDef) Mitigation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AssayTip/AssayCup Tray-used on the cobas e 801 module which is Recalled by...
The Issue: AssayTips part of the AssayTip/AssayCup Tray Tips used on the cobas e 801...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMED Oral Dispensers Recalled by Baxter Healthcare Corporation Due to...
The Issue: Exactamed 5 mL Oral Dispenser Pharmacy Packs may contain both 5 mL and 3 mL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZEUS ELISA Parvovirus B19 IgM Test System Recalled by Zeus Scientific, Inc....
The Issue: FDA inspection identified that due to increased positivity (false positives)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian Multileaf Collimator [MLC] Recalled by Varian Medical Systems, Inc....
The Issue: After a recent upgrade to the collimator software version 8.5, the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Nexframe Stereotactic System and StealthStation Cranial software...
The Issue: Entry point and lead placement inaccuracies during deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esthetic Abutment CC RP 1.5 mm pre-manufactured prosthetic components...
The Issue: Packages of abutments may contain an incorrect screw. While the screw will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temporary Abutment Engaging CC RP pre-manufactured prosthetic components...
The Issue: Packages of abutments may contain an incorrect screw. While the screw will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Base CC RP 1.5 mm Recalled by Nobel Biocare Usa Llc Due to...
The Issue: Packages of abutments (universal base) may contain an incorrect screw. While...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temporary Snap Abutment Engaging CC RP 1.5 mm Recalled by Nobel Biocare Usa...
The Issue: Packages of abutments may contain an incorrect screw. While the screw will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temporary Abutment Non-Engaging CC RP pre-manufactured prosthetic components...
The Issue: Packages of abutments may contain an incorrect screw. While the screw will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.