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. 2,644 recalls have been distributed to Iowa in the last 12 months.
Showing 3521–3540 of 28,127 recalls
Recalled Item: Auxiliary Common Gas Outlet (ACGO) conversion/install kits sold under...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire View. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ion Endoluminal System Recalled by Intuitive Surgical, Inc. Due to There is...
The Issue: There is a potential that the robotic system's instrument cart arm may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NavaClick Syringe and Needle Recalled by LINEAGE BIOMEDICAL, INC Due to...
The Issue: Incorrect GTIN number on carton.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer Recalled by Beckman...
The Issue: Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guidewire 70cm x 1mm (0.038 ) These accessories Recalled by Bard Peripheral...
The Issue: Due to guidewires being manufactured incorrectly with the guidewires being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Mishima...
The Issue: Due to a software issues, after the instrument processes 250 racks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VITROS XT Chemistry Products ALB-TP Slides is a single Recalled by...
The Issue: The reason for this recall is QuidelOrtho has determined that during normal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DLP Single Stage Venous Cannulae with right angle metal tip...
The Issue: During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BKIT BD Pyxis QFill Replenishment Station Recalled by CareFusion 303, Inc....
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis QFill Replenishment Station Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGrath Mac Video Laryngoscope Recalled by Covidien Due to Battery...
The Issue: Battery management system within Laryngoscope devices may deplete below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covideien McGRATH MAC Video Laryngoscope Recalled by Covidien Due to IFU...
The Issue: IFU update to address device's battery handling information.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGRATH" MAC EMS Video Laryngoscope Recalled by Covidien Due to Battery...
The Issue: Battery management system within Laryngoscope devices may deplete below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurora 4 Series Recalled by DKK Dai-Ichi Shomei Co., Ltd. Due to The weld on...
The Issue: The weld on the light head frame can crack which could lead to problems such...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurora Series Recalled by DKK Dai-Ichi Shomei Co., Ltd. Due to The weld on...
The Issue: The weld on the light head frame can crack which could lead to problems such...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurora 3 Series Recalled by DKK Dai-Ichi Shomei Co., Ltd. Due to The weld on...
The Issue: The weld on the light head frame can crack which could lead to problems such...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurora 2 Series Recalled by DKK Dai-Ichi Shomei Co., Ltd. Due to The weld on...
The Issue: The weld on the light head frame can crack which could lead to problems such...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Kiestra Urine Culture Application Powered by BD Synapsys Informatics...
The Issue: There is a potential risk that the image colony count does not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruDi NAV Suction Recalled by Integra LifeSciences Corp. Due to Specific...
The Issue: Specific lots of TruDi NAV Suction Instruments 0 Degrees were incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.