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. 2,556 recalls have been distributed to Iowa in the last 12 months.
Showing 14721–14740 of 28,127 recalls
Recalled Item: The LivaNova VNS Therapy System Recalled by LivaNova USA Inc Due to Lead...
The Issue: Lead impedance values reported by the affected VNS generator will be higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare 9805 and 9805P Hydraulic Patient Lifts Recalled by Invacare...
The Issue: Invacare has identified via customer complaints, the potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revanesse Versa Recalled by Prollenium Medical Technologies Inc. Due to...
The Issue: Labeling error. The product is labeled with an 18 month expiration date,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various GE Magnetic Resonance System on-site software version Product Usage:...
The Issue: Possible incorrect software version loaded.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroSet XT Injectable HA Bone Cement Recalled by Howmedica Osteonics Corp....
The Issue: Incorrect expiry date of 17-Dec-19 Correct expiry date is 11-Aug-19
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroSet XT Injectable HA Bone Cement Recalled by Howmedica Osteonics Corp....
The Issue: Incorrect expiry date of 9-Feb-20 Correct expiry date is 30-Aug-19
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Standard Percutaneous Antenna with Thermosphere Technology...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Long Percutaneous Antenna with Thermosphere Technology...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Short Percutaneous Antenna with Thermosphere Technology...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow CVC 2 Lumen Recalled by Arrow International Inc Due to The lidstock...
The Issue: The lidstock states the incorrect priming volume and flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Staclot LA 20 () The Staclot¿ LA and Staclot¿ Recalled by Diagnostica Stago,...
The Issue: There have been reports of shortened (T1-T2) results, where some instances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Staclot¿ LA () The Staclot¿ LA and Staclot¿ LA Recalled by Diagnostica...
The Issue: There have been reports of shortened (T1-T2) results, where some instances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDS Light Suspension Recalled by Stryker Communications Due to There is a...
The Issue: There is a potential the joint in the suspension of the device is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Systems Software Version 9.01 Update Kit. Recalled by bioMerieux,...
The Issue: The VITEK¿ 2 Systems Software Version 9.01 software may display incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empower FastLoad CT Syringe Pack -sterile disposable syringe kit for...
The Issue: Insufficient seal on the sterile barrier of the device, compromising the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bucky Stand SU-4000 Input 2017.11.17. SU41711085 Date: 2017-11-17 Recalled...
The Issue: Unintentional U-Arm movement
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Volcano FFR software used in the following systems connected...
The Issue: Interoperability issue that affects certain systems that use the recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Singles carbides by Meisinger Recalled by Hager & Meisinger Gmbh Due to...
The Issue: Incorrect packaging; There is a potential that a 1.0 mm carbide blade was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stationary Fluoroscopic X-ray System CombiDiagnost R90 Recalled by Philips...
The Issue: kV/mA lockin not functioning as specified which may result in the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS T2X table Recalled by Deerfield Imaging, Inc. Due to Table may drift...
The Issue: Table may drift in the roll position while in use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.