Nonsterile convenience kit: regard Item #830014016 — Class II medical device recall Z-1408-2022
Terminated recall by ROi CPS LLC, reported 2022-07-27. Some nonsterile components that were supposed to be sterile were packaged in nonsterile kits.
| Recall number | Z-1408-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ROi CPS LLC, Republic, MO, United States |
| Recall initiated | 2022-06-03 |
| Classified | 2022-07-19 |
| Reported by FDA | 2022-07-27 |
| Terminated | 2023-04-14 |
| Quantity | 40 kits |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10194717110156 |
| Lot numbers | 92605 |
| Model numbers | 830014016, LD00199PC |
| Expiration dates | 2023-08-31 |
Product
Nonsterile convenience kit: regard Item #830014016, LD00199P - C Section Mother.
Reason for recall
Some nonsterile components that were supposed to be sterile were packaged in nonsterile kits.
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-1408-2022. 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.