(a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm,… — Class II medical device recall Z-0833-2022
Terminated recall by Carefusion 2200 Inc, reported 2022-04-06, distributed nationwide. The finished device package did not contain the IFU.
| Recall number | Z-0833-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Carefusion 2200 Inc, Vernon Hills, IL, United States |
| Recall initiated | 2022-02-23 |
| Classified | 2022-03-30 |
| Reported by FDA | 2022-04-06 |
| Terminated | 2023-05-02 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, TW |
| Quantity | 152 units |
| UPC / GTIN / UDI-DI | 10885403153341, 10885403153358, 10885403155314, 10885403155321 |
| Lot numbers | 864909, B18XRD, C17XRD, C18XRD, C19XRD, D18XRD, D20XRD, G18XRD, G20XRD, J19XRD, K17XRD, K19XRD, XRDV09, XRDV10, XRDX02, XRDX06, XRDZ07 |
| Model numbers | 88-5910, 88-5920, 88-9808, 88-9809 |
Product
(a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog #88-5910; (b) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 5 mm, 30 degrees 7", 17.5 cm, Catalog #88-5920; (c) CareFusion Snowden-Pencer MIS, Endoplastic Fitting, Storz Scope, Catalog #88-9808; and (d) CareFusion Snowden-Pencer MIS, Endoplastic Fitting, Wolf Scope, Catalog #88-9809.
Reason for recall
The finished device package did not contain the IFU.
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-0833-2022. 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.