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. 2,469 recalls have been distributed to Delaware in the last 12 months.
Showing 23461–23480 of 27,373 recalls
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical TAMPA CATHETER 5 French 33 cm. Intended for Recalled by...
The Issue: Sterility of the device may be compromised due to unsealed pouch
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS (R) Chemistry Products FS Calibrator 1 Recalled by Ortho-Clinical...
The Issue: Calibrator values assigned for the calibrator kit lots were released using a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Infinix X-Ray Interventional System INFX-8000V/UU. An X-Ray system...
The Issue: Although the Flat Panel Detector (FPD) touch sensor is activated during use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS (R) Chemistry Products Calibrator Kit 17 Recalled by Ortho-Clinical...
The Issue: Calibrator values assigned for the calibrator kit lots were released using a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mobilett XP Digital Mobile X-ray System Product Usage: The Recalled...
The Issue: There is a potential fire hazard of certain Lithium-Ion batteries in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Ysio Systems Product Usage: The Ysio (New RAD-FAMILY) systems...
The Issue: Excessive usage of cleaning liquid on Siemens Ysio Systems may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Ventilator Flexport Interface Recalled by Spacelabs...
The Issue: Spacelabs Healthcare is voluntarily recalling the Hamilton Galileo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.