PlainRecalls
FDA Devices Moderate Class II Terminated

novaplus, General Purpose Kit, Cat. No. 56603

Reported: June 30, 2021 Initiated: May 11, 2021 #Z-1947-2021

Product Description

novaplus, General Purpose Kit, Cat. No. 56603

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

Details

Units Affected
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.
Location
Arden, NC

Frequently Asked Questions

What product was recalled?
novaplus, General Purpose Kit, Cat. No. 56603. Recalled by Medical Action Industries, Inc. 306. Units affected: 21 cases of 20 units.
Why was this product recalled?
There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
Which agency issued this recall?
This recall was issued by the FDA Devices on June 30, 2021. Severity: Moderate. Recall number: Z-1947-2021.