PlainRecalls
FDA Devices Moderate Class II Terminated

Cardiac Pack - LF, Model DYNJ31903I - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.

Reported: January 13, 2021 Initiated: November 13, 2020 #Z-0783-2021

Product Description

Cardiac Pack - LF, Model DYNJ31903I - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.

Reason for Recall

The cylindrical sponge component is not x-ray detectable.

Details

Recalling Firm
Medline Industries Inc
Units Affected
360
Distribution
Foreign distribution only - Canada.
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
Cardiac Pack - LF, Model DYNJ31903I - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.. Recalled by Medline Industries Inc. Units affected: 360.
Why was this product recalled?
The cylindrical sponge component is not x-ray detectable.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 13, 2021. Severity: Moderate. Recall number: Z-0783-2021.