FilmArray Pneumonia Panel (Penumo) REF RFIT-ASY-0144
FDA Recall Z-1944-2021 · Posted None
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Recalling FirmBioFire Diagnostics, LLC
Recall StatusTerminated
Product CodeQBH
Date Initiated2021-04-16
Date Terminated2024-04-02
Product Quantity9 kits (U.S. only)
Reason for Recall
Elevated rates of false positive/false negative and control failures while using the Pneumonia Panel, due to issues identified in the manufacturing process.
Firm Action
On 04/16/2021, the firm sent an "URGENT: MEDICAL DEVICE RECALL" Notification Letter via email informing its customers of an issue identified in the manufacturing process which might contribute to elevated rates of false positive/false negative results and control failures while using the pneumonia panel.
Customer are instructed to:
1) Immediately examine their inventory for product identified in this recall.
2) Discontinue use and discard any remaining product in their possession that is subject to this recall. The Recalling Firm will replace the product at no charge in accordance with its standard limited warranty.
3) Confirm the amount of pouches scrapped (if any) on the attached Acknowledgement of Receipt Form.
4) If the affected products have been further distributed, customers are to identify any recipients and notify them at once of this product recall.
5) Complete the accompanying Field Action Acknowledgment of Receipt Form and return to Recalling Firm so that it may acknowledge their receipt of this notification.
For questions or concerns contact Customer Support Department at [email protected] or via telephone 1-800-735-6544, option 5 for Product Technical Support.
Root Cause
Under Investigation by firm
Distribution Pattern
U.S. Nationwide distribution in the states of MN and OK. O.U.S.: None
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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