PlainRecalls
FDA Devices Moderate Class II Ongoing

Acceava Respiratory Strep A, CLIA Waived, Catalog Number 4580295008

Reported: September 25, 2024 Initiated: August 20, 2024 #Z-3185-2024

Product Description

Acceava Respiratory Strep A, CLIA Waived, Catalog Number 4580295008

Reason for Recall

Due to a classification error in our inventory management system, these medical devices were shipped to customers that did not have the requisite license to purchase such devices.

Details

Units Affected
5 kits
Distribution
US Nationwide distribution.
Location
Richmond, VA

Frequently Asked Questions

What product was recalled?
Acceava Respiratory Strep A, CLIA Waived, Catalog Number 4580295008. Recalled by Cypress Medical Products LLC. Units affected: 5 kits.
Why was this product recalled?
Due to a classification error in our inventory management system, these medical devices were shipped to customers that did not have the requisite license to purchase such devices.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 25, 2024. Severity: Moderate. Recall number: Z-3185-2024.