Search
Returning search results with filters:
Remove filter for
Issue: Manufacturing defect
Remove filter for
Recall class: Type I
Remove filter for
Type: Recall
Clear all
Type
Audience
Category
Issue
Last updated
Recall class
Please note: using the search filters may not provide accurate search results for records prior to November 2021. When searching for older records, please ensure that you use the include archived checkbox.
Displaying 1 - 4 of 4 items.
Liquiband Fix8 Open Hernia Mesh Fixation Device
During verification testing, a non-conformance was detected. Failure mode was uncontrolled leakage of glue from the distal tip of the Fix8 open (FX002) device.
Recall start date: Feb 3, 2022
RecallHealth product recall | 2022-02-14
Intelect-Chattanooga Ultrasound Products
All ultrasound gels and lotions manufactured by Eco-Med are at risk for bacterial contamination. Multiple products could be affected by manufacturing issues associated with the company's ultrasound gel (such as inappropriate testing of finished product,…
RecallHealth product recall | 2021-12-20
Intelect mobile products
All ultrasound gels and lotions manufactured by Eco-Med are at risk for bacterial contamination. multiple products could be affected by manufacturing issues associated with the company's ultrasound gel (such as inappropriate testing of finished product,…
RecallHealth product recall | 2021-12-07
Puritan Bennett 980 Series Ventilator
This voluntary medical device correction is being taken following the investigation of six customer reports stating that a total of four ventilators became inoperable during use. One of these reports indicated that, following the ventilator becoming…
RecallHealth product recall | 2021-11-29