Recall Z-0147-2022— Medical Action Industries, Inc. 306

Class II · Terminated

Class II FDA medical device recall by Medical Action Industries, Inc. 306, initiated 2021-09-08, terminated 2023-10-13. FDA's recall record names no specific 510(k) clearance for this event. Product: Kit: Central Line Dres Change 20/Cs. Reason: The ChloraPrep 3ml kit component has a shorter expiry date than the labeled kit expiry date..

Recalling firm
Medical Action Industries, Inc. 306
Classification
Class II
Status
Terminated
Initiated
2021-09-08
Terminated
2023-10-13
Firm location
Arden, NC, United States

Product description

Kit: Central Line Dres Change 20/Cs

Reason for recall

The ChloraPrep 3ml kit component has a shorter expiry date than the labeled kit expiry date.

Data sourced from openFDA. This site is unofficial and independent of the FDA.