Z-1949-2021 Class II Terminated

Recalled by Medical Action Industries, Inc. 306 — Arden, NC

FDA device recall Z-1949-2021 was initiated by Medical Action Industries, Inc. 306 on May 11, 2021 and is designated Class II. 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 The recall status is terminated (terminated May 10, 2023). Affected quantity: 31 cases of 20 units.

Recall Details

Product Type
Devices
Report Date
June 30, 2021
Initiation Date
May 11, 2021
Termination Date
May 10, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
31 cases of 20 units

Product Description

Medical Action INDUSTRIES INC., Minor Procedure Tray, REF 61214

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

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.

Code Information

Batch Numbers: 0000275137, Exp. 05/29/2022; 0000276914, Exp. 02/01/2023