Data Foundry

Medical device recalls 2022

regard MAJOR EAR — Class II medical device recall Z-0293-2023

Terminated recall by ROi CPS LLC, reported 2022-11-30, distributed in FL, LA, MO, NC. Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.

Recall numberZ-0293-2023
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmROi CPS LLC, Republic, MO, United States
Recall initiated2022-10-20
Classified2022-11-23
Reported by FDA2022-11-30
Terminated2026-04-01
DistributedFL, LA, MO, NC
Quantity200 kits
UPC / GTIN / UDI-DI10194717079958
Lot numbers91205, 92037
Model numbers800070010
Expiration dates2023-01-31, 2023-06-30

Product

regard MAJOR EAR, ET00326J, Item Number 800070010; ear surgery convenience kit

Reason for recall

Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.

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-0293-2023. 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.