Reported Oct 21, 2026 · Ongoing · Updated Oct 26, 2026
Generic Name: BioFire¿ Joint Infection (JI) Panel Generic Name: BioFire¿ Joint Infection (JI) Panel Model/Catalog…
BioFire Diagnostics, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: BioFire Diagnostics, LLC · 515 S Colorow Dr · Salt Lake City, UT · 84108-1248
Is this the product you have?
- Generic NameBioFire¿
- Joint Infection (JI) Panel Generic NameBioFire¿ Joint Infection (JI)
- Panel Model/Catalog NumberRFIT-ASY-0138 (30 Kit)
- RFIT-ASY-0135 (6 Kit) Software VersionN/A
- Product DescriptionMulitple-type osteoarticular pathogen nucleic acid IVD, kit
- nucleic acid technique (NAT) ComponentN/A
- Lot codes and dates
3 of 3 products
Products covered by this recall # Barcodes Product as published 1 0081538102019200815381020208Lot Code: UDI Nos 00815381020192 (30 Kit), 00815381020208 (6 Kit) 2 Model Nos RFIT-ASY-0138 (30 Kit), RFIT-ASY-0135 (6 Kit) 3 Lot Numbers 0677326, 0806426, 0806526, 1289126, 1289226, 1405526, 1405626, 1413026, 1413426, 1413526, 1507826, 1613326, 1684726 - Amount recalled
- 1,186
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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