Product Recalls in Iowa
Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,364 recalls have been distributed to Iowa in the last 12 months.
Showing 42341–42360 of 49,990 recalls
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan -Neg Breakpoint Combo Panel Type 34 Recalled by Beckman Coulter,...
The Issue: Siemens Healthcare Diagnostics has received complaints regarding panel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...
The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oasis TEARS Recalled by Oasis Medical Inc Due to Labeling: Missing Label;...
The Issue: Labeling: Missing Label; The label on the immediate bottle is missing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Poco Pac Salad Dressing Recalled by Diamond Crystal Brands, Inc. Due to...
The Issue: Undeclared Allergen: Egg
Recommended Action: Do not consume. Return to store for a refund or discard.
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: DeVilbiss Model DV5x Series CPAP units. For use in treating Recalled by...
The Issue: A limited number of DV5x Series CPAP units were manufactured and shipped...
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.