Data Foundry

Medical device recalls 2022

Accelerate PhenoTest BC kit REF 10102018 — Class II medical device recall Z-0346-2023

Ongoing recall by Accelerate Diagnostics Inc, reported 2022-12-07, distributed in AR, CA, DC, FL, GA, IA, IL, IN…. Due improperly formulated and released bulk lot of fluorescence in situ hybridization (FISH) probes resulting

Recall numberZ-0346-2023
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmAccelerate Diagnostics Inc, Tucson, AZ, United States
Recall initiated2022-10-17
Classified2022-11-30
Reported by FDA2022-12-07
DistributedAR, CA, DC, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, MO, MS, MT, NC, ND, NJ, NY, OH, PA, RI, SC, TN, TX, VA, WA, WV
Countries outside the USAE, DE, ES, IT, KW, LV, PL, PT, RO, SA
Quantity7,160 kits
Pathogensstaphylococcus
UPC / GTIN / UDI-DI00862011000369
Lot numbers5546A, 5548A, 5550A, 5551A, 5553A, 5554A, 5555A, 5556A, 5557A, 5558A, 5559A, 5560A, 5561A, 5562A, 5563A, 5564A, 5567A, 5568A, 5570A, 5571A, 5572A, 5574A, 5576A, 5577A, 5578A, 5579A, 5580A, 5581A, 5582A, 5583A, 5585A, 5586A, 5587A, 5589A, 5590A, 5591A, 5592A, 5594A, 5595A, 5596A and 13 more
Model numbers10102018

Product

Accelerate PhenoTest BC kit REF 10102018

Reason for recall

Due improperly formulated and released bulk lot of fluorescence in situ hybridization (FISH) probes resulting in false positive identification results for Staphylococcus aureus and Streptococcus spp.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0346-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.