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. 2,618 recalls have been distributed to Iowa in the last 12 months.
Showing 10161–10180 of 28,127 recalls
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America Llc Due to...
The Issue: Manufacturing failed to follow process steps resulting in the distribution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom Ophthalmic Surgical Procedure Packs Recalled by Alcon Research,...
The Issue: Reports have been received concerning mold found on gowns included in custom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Feth-R-Kath Catheter Recalled by Epimed International, Inc. Due to Outer...
The Issue: Outer coating of the catheter may deteriorate and result in the coating to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Velocity Disposable Bipolar Ablators - Product Usage: intended to be...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Disposable Bipolar Ablators - Product Usage: intended to be Recalled...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HNM Disposable Bipolar Ablators - Product Usage: intended to be used for...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-Series Equipment Management System Recalled by Stryker Communications Due...
The Issue: The manufacturer has become aware that there is a likelihood that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Basic (N) 180-Drager Breathing Circuits/Anesthesia Sets Order...
The Issue: Y-piece may become detached from the ventilation hose either before or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia gas-machine - Product Usage: intended for use in administering...
The Issue: Maquet Critical Care AB received complaints where the FiCO2 value was not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Watertrap (N) 180-Drager Breathing Circuits/Anesthesia Sets Order...
The Issue: Y-piece may become detached from the ventilation hose either before or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Anesthesia (N) 180 - Drager Breathing Circuits/Anesthesia Sets...
The Issue: Y-piece may become detached from the ventilation hose either before or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic (N) 180- Drager Breathing Circuits/Anesthesia Sets Order...
The Issue: Y-piece may become detached from the ventilation hose either before or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma)...
The Issue: Due to two (2) issues: 1) The firm distributed COVID-19 Rapid Test Cassettes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orient Gene COVID- 19 IgG/ IgM Rapid Test Cassette (Whole Recalled by...
The Issue: Due to two (2) issues: 1) The firm distributed COVID-19 Rapid Test Cassettes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolve Cell Culture Bags Recalled by OriGen Biomedical, Inc. Due to It was...
The Issue: It was identified that tissue culture bags were incorrectly labeled as free...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duodenoscope and accessories Recalled by Olympus Corporation of the Americas...
The Issue: Olympus Medical Systems Corporation (OMSC) has received complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...
The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...
The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preventative Maintenance Kits G5010007) and spare part kits (G5064801 and...
The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit - Product Usage: Used for Continuous Renal Recalled...
The Issue: Variability in the performance of the tubing in the Prismaflex Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.