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. 2,447 recalls have been distributed to Iowa in the last 12 months.
Showing 25441–25460 of 28,127 recalls
Recalled Item: Medtronic Custom Perfusion System with Carmeda BioActive Surface. Model...
The Issue: Medtronic was notified that Edwards Lifesciences has initiated a product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Perfusion System. Model Numbers: 1D80R8 Recalled by...
The Issue: Medtronic was notified that Edwards Lifesciences has initiated a product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is labeled in part: LIST NO. 43449 Recalled by Hospira Inc. Due to...
The Issue: Hospira has recieved reports that the vacuum needed to create suction with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemoccult II BRAND SENSA elite Recalled by Assuramed Due to The products may...
The Issue: The products may have been stored at temperatures outside their required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT and Brilliance iCT SP These systems are intended Recalled by...
The Issue: An artifact that resembles thrombus may appear on the image.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProTime Microcoagulation System Recalled by Assuramed Due to The products...
The Issue: The products may have been stored at temperatures outside their required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PleuraGuide Disposable Chest Tube Kit Recalled by Atrium Medical Corporation...
The Issue: Individual component's IFUs are not included with the kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAC Pneumatic Retraction Arm. A support arm used to hold Recalled by...
The Issue: Changes were implemented to the UNITRAC instructions for use to ensure safe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moore Hip Prosthesis Long Fenestrated Stem Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer recently conducted a review of historic packaging validations...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemoCue¿ Urine Albumin Microcuvettes Recalled by HemoCue AB Due to HemoCue...
The Issue: HemoCue AB has become aware of a production related problem involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DiaScreen Liquid Urine Controls: Positive and Negative Assayed Liquid...
The Issue: The products may have been stored at temperatures outside their required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards EndoReturn Arterial Cannula Recalled by Edwards Lifesciences, LLC...
The Issue: Edwards Lifesciences is recalling certain lots of the EndoReturn Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Max Glucose Test Strips (10 Count Boxed) Catalog Number: Recalled by...
The Issue: Reports of false abnormally high glucose readings from test strips
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Max Glucose Test Strips (10 Count Vials) Catalog Number: Recalled by...
The Issue: Reports of false abnormally high glucose readings from test strips
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Max Plus Monitor System (Kit w/10 Count Vials Canada) Recalled by Nova...
The Issue: Reports of false abnormally high glucose readings from test strips
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemoCue¿ Glucose 201 Microcuvettes Recalled by HemoCue AB Due to During a...
The Issue: During a complaint investigation HemoCue AB discovered punctured HemoCue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Max Plus Monitor System (Kit w/10 Count Vials) Catalog Recalled by Nova...
The Issue: Reports of false abnormally high glucose readings from test strips
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Max Glucose Test Strips (50 Count DME) Catalog Number: Recalled by Nova...
The Issue: Reports of false abnormally high glucose readings from test strips
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Max Glucose Test Strips (100 Count Retail Canada)Catalog Number:...
The Issue: Reports of false abnormally high glucose readings from test strips
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Max Plus Monitor System (Kit w/10 Count Vials International) Recalled...
The Issue: Reports of false abnormally high glucose readings from test strips
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.