Z-1946-2021 Class II Terminated
FDA device recall Z-1946-2021 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: 97 boxes of 20 devices.
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
- 97 boxes of 20 devices
Product Description
Medical Action INDUSTRIES INC., Disposable Instrument Pack Curved Hemostat, REF 56224
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: 0000277592, Exp. 10/12/2025; 0000274266, Exp. 07/21/2025; 0000275098, Exp. 08/21/2025; 0000276380, Exp. 09/24/2025