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 3541–3560 of 28,127 recalls
Recalled Item: IBA Proton Therapy System - PROTEUS 235 ProteusPLUS and ProteusONE Recalled...
The Issue: Safety Parameters Verification Mechanisms can be deactivated in clinical runtime
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GM60A. Digital Diagnostic Mobile X-Ray System. Recalled by NeuroLogica...
The Issue: Potential for the anti-fall system of the device arm to fail.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Salivary Testosterone ELISA Model/Catalog Number: SLV-3013...
The Issue: Invalid Controls. The Low Control is out of range; too high which causes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FRT250 - 4.0-6.4 CARTRIDGE. Component of the Fassier-Duval Telescopic IM...
The Issue: During the assembly of the FRT250 cartridge assembly, an incorrect component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic VITROS Folate Reagent Pack 1/2 Recalled by...
The Issue: It was confirmed that fibrinogen in patient plasma samples precipitates out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement Configured for...
The Issue: Devices were labeled with an expiration date of four years and ten days...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B in combination with Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe systems with software version VD15B-Intended to be used Recalled...
The Issue: If the Sensis documentation functionality is used during adding of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPince Ultra Full Core Biopsy Instrument: : 360-1080-01 Recalled by Argon...
The Issue: Holes have been identified in biopsy instrument packaging trays compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable 5 Lead Cable and Lead Wire System Recalled by Stryker...
The Issue: Disposable 5 lead cable and lead wire system package that should contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMINOS Lotus Max -Intended to visualize anatomical structures by converting...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile Max -Intended to visualize anatomical structures by converting...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF Max- Intended to visualize anatomical structures by converting...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multitom Rax -Intended to visualize anatomical structures by converting an...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT Hip Joint Metal/Polymer Semi-Constrained Cemented Prosthesis Recalled by...
The Issue: Affected product has an increased risk of postoperative perisprosthetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...
The Issue: Due to packaging defects, sterility assurance and heparin activity may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...
The Issue: Due to packaging defects, sterility assurance and heparin activity may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobra Recalled by Neurovision Medical Products Inc Due to Mislabeling
The Issue: mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.