RecallDepth

Laparoscopy CDS

Company
Medline Industries, Inc.
Recall Initiated
April 12, 2017
Terminated
August 5, 2019
Recall Number
Z-2978-2018
Quantity
15 kits
Firm Location
Waukegan, IL

Reason for Recall

One manufacturing lot of a non-sterile pack was assembled with a non-sterile component labeled sterile (kit component #80532NS). The non-sterile component 80532NS was supposed to be placed inside the sterile portion of the pack where it would subsequently be exposed to the ethylene oxide sterilization process. However, the component was not placed in the sterile portion of the pack during assembly and was never exposed to the sterilization process. Component 80532NS was inadvertently released non-sterile. Component 80532NS is packaged by Medline and is an Anti-fog kit that contains 1 bottle of 6g Anti-Fog solution and an adhesive backed sponge.

Distribution

CA, NM

Lot / Code Info

Model: CDS920114F. Lot: 17MB5499

Root Cause

Under Investigation by firm

Action Taken

Firm contacted customers via phone and letter beginning April 12, 2017. Customers were instructed to remove the Ethicon BioPatch Protective Disk with CHG from the kit(s) and return it to the firm. The firm would provide a sterile replacement BioPatch. Affected product will be destroyed.

More recalls by Medline Industries, Inc.

View all recalls by this company →