Skip to the content

FDA Medical Device Recalls (openFDA)

Qvella Corporation: The FAST System and the FAST PBC Prep Cartridge together are a closed, rapid and automated sample preparation system for isolating bacterial cells directly from a positive blood culture (PBC). The cartridge and instrument isolate and concentrate bacterial cells directly from PBC by removing blood, cellular and culture media matrix components from the sample, thereby reducing the sample volume considerably while maintaining bacterial cell viability. The resulting material is a purified microbial suspension or Liquid Colony for use in downstream in vitro diagnostics.

Recall number
Z-0425-2023
Recalling firm
Qvella Corporation
Product
The FAST System and the FAST PBC Prep Cartridge together are a closed, rapid and automated sample preparation system for isolating bacterial cells directly from a positive blood culture (PBC). The cartridge and instrument isolate and concentrate bacterial cells directly from PBC by removing blood, cellular and culture media matrix components from the sample, thereby reducing the sample volume considerably while maintaining bacterial cell viability. The resulting material is a purified microbial suspension or Liquid Colony for use in downstream in vitro diagnostics.
Status
Open, Classified
Initiated
2022-11-02
Posted
2022-12-07
Terminated
not on file
Reason
Device exceeds the limitations of a Class I 510(k)-exempt device so the user manual, instructions for use, and promotional materials are being corrected to remove all references to downstream applications.
Root cause
No Marketing Application
Action
On 11/02/22, recall notices were emailed to customers who were asked to discard all product labeling materials (i.e., user manual, instructions for use, product brochures, etc.) received to date from the recalling firm until new labeling materials are provided. Please respond to the email with the attached recall notice as follows "have read and understood the intended use and indications for use of FAST System and PBC Prep Cartridges." Customers with additional questions are asked to contact Technical Support at (833) 478-3552, TechSupport@qvella.com
Quantity
1868
Distribution
US: CA, NY, AL, UT
Lot, serial or model codes
TSP-UM-001, Revisions: 2 and 3; MKT-0025, Revisions: 2 and 3; TSP-PI-001, Revisions: 2 and 3
510(k) numbers
not on file
PMA numbers
not on file
Product code
JJH
Firm FEI
3013825847
Firm city
Richmond Hill
Firm state
not on file
Firm country
Canada

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

Search this register