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. 2,664 recalls have been distributed to Iowa in the last 12 months.
Showing 381–400 of 49,990 recalls
Recalled Item: CellMek SPS Sample Preparation System Recalled by Beckman Coulter, Inc. Due...
The Issue: Sample preparation system designed to automate staining, lysing, cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Swiss Chocolate Cake Mix Recalled by B.C. Williams Bakery Service, Inc Due...
The Issue: Undeclared Milk Allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON...
The Issue: These lots of reprocessed catheters may contain small particles of residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10...
The Issue: These lots of reprocessed catheters may contain small particles of residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry...
The Issue: These lots of reprocessed catheters may contain small particles of residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters:...
The Issue: These lots of reprocessed catheters may contain small particles of residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LSL Healthcare Recalled by LSL Healthcare Inc. Due to BD ChloraPrep Triple...
The Issue: BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Information Center iX Recalled by Philips North America Due to A...
The Issue: A recent software (SW) patch modifies Mobile Event Notification filter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed St. Jude Supreme and Response Diagnostic Electrophysiology...
The Issue: These lots of reprocessed catheters may contain small particles of residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Water for Irrigation Recalled by Baxter Healthcare Corporation Due...
The Issue: Presence of particulate matter: plastic particles from the bottle rim were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium Topical Gel Recalled by Cipla USA, Inc. Due to Failed PH...
The Issue: Failed PH Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE...
The Issue: These lots of reprocessed catheters may contain small particles of residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters:...
The Issue: These lots of reprocessed catheters may contain small particles of residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clearest Strep-A Cassette Test. Test to determine the presence of Recalled...
The Issue: Product not cleared by the FDA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 20mm x 10mm...
The Issue: Increased reports of stent deployment and expansion issues. The most common...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm Recalled...
The Issue: Increased reports of stent deployment and expansion issues. The most common...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wegovy (semaglutide) Injection Recalled by Novo Nordisk Inc. Due to Presence...
The Issue: Presence of Particulate Matter: Hair was found in a prefilled syringe
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wegovy (semaglutide) Injection Recalled by Novo Nordisk Inc. Due to Presence...
The Issue: Presence of Particulate Matter: Hair was found in a prefilled syringe
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: traZODONE Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA) Inc...
The Issue: Failed Tablet/Capsule Specifications: Product complaint received that some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 8mm x 8mm...
The Issue: Increased reports of stent deployment and expansion issues. The most common...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.