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. 2,571 recalls have been distributed to Iowa in the last 12 months.
Showing 14321–14340 of 28,127 recalls
Recalled Item: Truliant Tibial Fit Tray Cemented SZ 3F / 3T Recalled by Exactech, Inc. Due...
The Issue: 2.5 Truliant Fit Trays were mismarked as 3
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS II SUTURE 18"(45CM) 2-0 VIO Product Code:Z739D - PDS Recalled by...
The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICRYL PLUS Sutures: VICRYL PLUS SUTURE 18"(45CM) 3-0 VIO VICRYL Recalled by...
The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICRYL Sutures VICRYL SUTURE 18"(45CM) 0 VIO VICRYL SUTURE 18"(45CM)...
The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Unity Recalled by Elekta Limited Due to Users need to be aware when...
The Issue: Users need to be aware when using these protocols for daily on line plan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beaver Xstar Slit Knife 2.4 mm Recalled by Beaver Visitec Due to Mislabeling
The Issue: Mislabeled. The package labeling indicates a size 2.4mm, 45 degree Double...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics Due...
The Issue: One of the software algorithms used to detect sample dispense errors was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RT Elements Software revisions of the RT Elements applications have Recalled...
The Issue: There is a potential for an incorrect dose distribution calculation by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salto Talaris Tibial Total Ankle Prosthesis Tray Recalled by Integra...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salto Talaris Tibial Ankle Prosthesis Tray Recalled by Integra LifeSciences...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades:Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salto Talaris Tibial Total Ankle Prosthesis Tray Recalled by Integra...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salto Talaris Tibial Total Ankle Prosthesis Tray Recalled by Integra...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.