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. 2,627 recalls have been distributed to Iowa in the last 12 months.
Showing 6921–6940 of 28,127 recalls
Recalled Item: cobas Influenza A/B & RSV UC (Utility Channel) Qualitative nucleic Recalled...
The Issue: The firm received customer complaints regarding false negative Influenza A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas SARS-CoV-2 & Influenza A/B Qualitative assay for use on Recalled by...
The Issue: The firm received customer complaints regarding false negative Influenza A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELAY PRO Recalled by Bolton Medical Inc. Due to The product may be shorter...
The Issue: The product may be shorter than packaging indicates
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELAY PRO Recalled by Bolton Medical Inc. Due to The product may be shorter...
The Issue: The product may be shorter than packaging indicates
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Monitor/ScanWatch Recalled by Withings Due to A software bug eliminated...
The Issue: A software bug eliminated the initial ECG activation and review of the ECG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may shut down unexpectedly due to blood entering in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may shut down unexpectedly due to blood entering in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOSTOP G BIORESORBABLE CEMENT RESTRICTOR Catalog Numbers: 546308000 (Size...
The Issue: All lots of BIOSTOP G Bioresorbable Cement Restrictor are being removed as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Low Flow Disposable Patient Circuit for the Precision Flow System Recalled...
The Issue: There have been reports of excessive condensation associated with certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroPICC 4Fr Single Lumen Recalled by Access Vascular, Inc Due to Select...
The Issue: Select catheter lots were identified to be labeled with incorrect expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroMID 4Fr Single Lumen - Basic Kit Recalled by Access Vascular, Inc Due...
The Issue: Select catheter lots were identified to be labeled with incorrect expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroPICC 4Fr Single Lumen Recalled by Access Vascular, Inc Due to Select...
The Issue: Select catheter lots were identified to be labeled with incorrect expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotome MammoStar Biopsy Site Identified Recalled by Carbon Medical...
The Issue: The label incorrectly identifies the product as STAR1401, a 1x3mm Barbell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaGuide Intelligent Ultrasound System Recalled by NovaSignal Corp. Due to...
The Issue: Transcranial Doppler/ultrasound system tablet has a faulty hard drive, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.