Data Foundry

Medical device recalls 2022

ORAcollect Dx — Class II medical device recall Z-0981-2022

Ongoing recall by DNA Genotek Inc., reported 2022-04-27, distributed nationwide. Evaporation of stabilizing liquid reducing shelf life.

Recall numberZ-0981-2022
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmDNA Genotek Inc., Kanata, Canada
Recall initiated2022-02-18
Classified2022-04-21
Reported by FDA2022-04-27
DistributedNationwide (US)
Countries outside the USAU, BE, BR, CA, CL, CN, DE, DK, FI, GB, HR, IT, JP, NL, TH, ZA
UPC / GTIN / UDI-DI00627595000309, 00627595000569
Lot numbersXI512, XI513, XI514, XI519, XI520, XI521, XI522, XI534, XJ536, XJ537, XK505, XK518, XK519, XL503, XL504, XL505, XL506, XL510, XL511, XL512, XL521, XL522, XL535, YA501, YA503, YA509, YA510, YA511, YA514, YA515, YA516, YA530, YA531, YA532, YB501, YB506, YB511, YB512, YB522, YB523 and 111 more

Product

ORAcollect Dx, Catalog Number/SKU: OCD-100, OCD-100A. Material numbers: OCD-100, OCD-100.008, OCD-100.012, OCD-100.014+ACP078, OCD-100.014+ACP078, OCD-100.032 and OCD-100A, OCD-100A.022, OCD-100A.023, OCD-100A.024, OCD-100A.025

Reason for recall

Evaporation of stabilizing liquid reducing shelf life.

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-0981-2022. 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.