Hologic, Inc.: Device Recall

Recall #Z-0694-2025 · 11/08/2024

Class II: Risk

Recall Details

Recall Number: Z-0694-2025
Classification: Class II
Product Type: Device
Recalling Firm: Hologic, Inc.
Status: Ongoing
Date Initiated: 11/08/2024
Location: San Diego, CA, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 3

Reason for Recall

SARS-CoV-2/Flu A/B/RSV Assay Kit may erroneously produce SARS-CoV-2 false positive results.

Product Description

Panther Fusion SARS-CoV-2/Flu A/B/RSV Assay, REF: PRD-07400

Distribution Pattern

US: AK

Other Recalls by Hologic, Inc.

Class II: Risk 12/12/2025

Fungal contamination of affected lot with Parengyodontium album.
Class II: Risk 01/15/2025

Devices presented a condition in which the inner needle separated from the hub and produced a longer throw of the inner needle or dislodgement.
Class II: Risk 01/08/2025

Three lots of Rapid fFN Specimen Collection kit (901164, 901165, and 904850) contain Rapid fFN Specimen Collection Tubes which may be empty, underfilled, or overfilled with extraction buffer. The transport tubes are used with the Fetal Fibronectin Enzyme Immunoassay and Rapid fFN¿ for the TLiIQ¿ System which aids in assessing the risk of preterm delivery. The use of empty transport tubes or transport tubes containing insufficient extraction buffer volume may result in invalid results and/or delays in obtaining results. Additionally, the use of underfilled tubes may result in false positive results and the use of overfilled tubes may result in false negative results.
Class II: Risk 12/13/2024

Potential weak pouch seal on Panther Fusion GBS assay cartridge, causing potential for invalid or incorrect results leading to a possible delay of treatment.
Class I: Dangerous 10/10/2024

Firm received reports of adverse events/complications that include serious injuries, such as pain, infection, rash, device migration, device erosion, seroma, and discomfort.

View all recalls by Hologic, Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.