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. 2,622 recalls have been distributed to Iowa in the last 12 months.
Showing 8821–8840 of 28,127 recalls
Recalled Item: smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE Recalled by Smith &...
The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE Recalled by Smith &...
The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew EVOS MEDIAL DISTAL FEMUR PLATE Recalled by Smith & Nephew, Inc....
The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol...
The Issue: When calibrating using the standard provided in the kit, the change in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diversatek Health Recalled by Diversatek Healthcare Due to M-Catch Retrieval...
The Issue: M-Catch Retrieval Nets, Part Number 1175-01 / Lot Number 001919, that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wireless Footswtich used with the following Philips Allura Xper and Recalled...
The Issue: Wireless foot switch connection issues causing interruption of Fluoroscopy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System:...
The Issue: The Instructions for Use have been updated to include: (1) Clarification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray...
The Issue: It was noticed in production on 28.10.2021, that the final testing database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 by...
The Issue: Due to consoles not in compliance with the latest electrical safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVLP Convenience Pack/Kit Recalled by Medline Industries Inc Due to NaCl 250...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous Access Pack-LF Convenience Kit Recalled by Medline Industries Inc Due...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Major Vascular CDS Convenience Kit Recalled by Medline Industries Inc Due to...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bedside PICC CDS Convenience Kit Recalled by Medline Industries Inc Due to...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Convenience Kit Recalled by Medline Industries Inc Due to NaCl 250 mL...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott HeartMate Touch Communication System Recalled by Thoratec Corp. Due...
The Issue: If LVAS communication system is trying to establish Bluetooth connection and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Ocean Water Seal Chest Drain is a plastic Recalled by Atrium Medical...
The Issue: Inadequate/inappropriate Set-Up Instructions, which may result in delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...
The Issue: If the system experiences an overvoltage / power surge it can cause a short...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...
The Issue: If the system experiences an overvoltage / power surge it can cause a short...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iDesign Recalled by AMO Manufacturing USA, LLC Due to Aberrometer and...
The Issue: Aberrometer and precision laser systems are affected by a remote code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.