FDA Recall Terminated

Cardiac Insulation Pad, OPEN HEART CDS

Recall: Z-2979-2018 · Initiated April 12, 2017

Recall

Recall Number
Z-2979-2018
Event Number
78411
Firm
Medline Industries, Inc.
FEI Number
3000717925
Product Code
N/A
Status
Terminated
Root Cause
Under Investigation by firm
Initiated
April 12, 2017
Terminated
August 5, 2019
Address
1170 S Northpoint Blvd, Waukegan, IL, 60085-6757

Description

Cardiac Insulation Pad, OPEN HEART CDS

Reason

Complete delivery System (CDS) # CDS984746C was assembled using a non-sterile cardiac insulation pad, Medline component number 32369. The non-sterile component (32369) was placed within the non-sterile portion of the CDS assembly. This component should have been placed inside the sterile portion of the pack where it would have subsequently been exposed to an ethylene oxide sterilization process. This component was not placed in the sterile portion of the pack and was not sterilized, resulting in the inadvertent release of this item in a non-sterile state. The contents of the sterile kit were properly sterilized and the remaining contents of the non-sterile subassembly had the appropriate sterility status based on their intended use.

Action

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.

Distribution

CA, NM

Quantity

77 kits