PlainRecalls
FDA Devices Moderate Class II Ongoing

Terragene Bionova PCD (PCD222-C)

Reported: February 7, 2024 Initiated: December 7, 2023 #Z-0837-2024

Product Description

Terragene Bionova PCD (PCD222-C)

Reason for Recall

Due to a discrepancy between the FDA-Cleared Indications for Use (IFU) and the actual IFU distributed with the products.

Details

Recalling Firm
TERRAGENE S.A.
Units Affected
80 stripes
Distribution
U.S. Nationwide distribution in the states of GA, IN, MI, MT, NY, PA, TX and VA.
Location
Alvear

Frequently Asked Questions

What product was recalled?
Terragene Bionova PCD (PCD222-C). Recalled by TERRAGENE S.A.. Units affected: 80 stripes.
Why was this product recalled?
Due to a discrepancy between the FDA-Cleared Indications for Use (IFU) and the actual IFU distributed with the products.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 7, 2024. Severity: Moderate. Recall number: Z-0837-2024.