FDA Medical Device Recalls (openFDA)
Medical Action Industries, Inc. 306: novaplus, General Purpose Kit, Cat. No. 56603
- Recall number
- Z-1947-2021
- Recalling firm
- Medical Action Industries, Inc. 306
- Product
- novaplus, General Purpose Kit, Cat. No. 56603
- Status
- Terminated
- Initiated
- 2021-05-11
- Posted
- not on file
- Terminated
- 2023-05-10
- Reason
- There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
- Root cause
- Process control
- 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.
- Quantity
- 21 cases of 20 units
- Distribution
- US Nationwide distribution in the states of OH, CO, CA, IL, FL, VA, TX, MN, GA, WA, MA, MD, NY, LA, AZ, OR.
- Lot, serial or model codes
- Batch Numbers: 0000275724, Exp. 02/15/2022; 0000277619, Exp. 04/15/2022
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- KDD
- Firm FEI
- 1030451
- Firm city
- Arden
- Firm state
- NC
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28