Xeridiem Mediem Medical Devices recalls

Xeridiem Mediem Medical Devices has 105 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 2 Mar 2016. The most frequent reason is packaging defects.

Total recalls105since 2016
Last 12 months0reported
Class I00% of total
Ongoing0latest 2 Mar 2016

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 105 100%Class III 0 0%

Why xeridiem mediem medical devices is recalled

Product types

By year

All xeridiem mediem medical devices recalls, newest first

105 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide
DeviceCLASS IIEndoVive 3s Low Profile Balloon Kits recalled by Xeridiem Mediem MedicalXeridiem Mediem Medical DevicesPackaging DefectsNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.