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Terminated

Medical Action INDUSTRIES INC., Disposable Instrument Pack Curved Hemostat, REF 56224

FDA Recall Z-1946-2021 · Posted None

Recalling FirmMedical Action Industries, Inc. 306
Recall StatusTerminated
Product CodeKDC
Date Initiated2021-05-11
Date Terminated2023-05-10
Product Quantity97 boxes of 20 devices

Reason for Recall

There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits

Firm Action

Medical Action Industries, Inc. initiated the recall by email on 05/11/2021 Distributors were instructed to notify their customers. The firm is requesting those in possession of the recalled articles discard them.

Root Cause

Process control

Distribution Pattern

US Nationwide distribution in the states of OH, CO, CA, IL, FL, VA, TX, MN, GA, WA, MA, MD, NY, LA, AZ, OR.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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