CareFusion Safe-T-Centesis Catheter Drainage Tray — Class II medical device recall Z-1795-2020
Terminated recall by Becton Dickinson & Company, reported 2020-05-06, distributed in AL, CO, IL, MA, MO, OK, RI, VA…. The 8 Fr catheter was manufactured with the 6.9 Fr needle instead of the 8 Fr needle.
| Recall number | Z-1795-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2020-03-26 |
| Classified | 2020-04-24 |
| Reported by FDA | 2020-05-06 |
| Terminated | 2020-08-21 |
| Distributed | AL, CO, IL, MA, MO, OK, RI, VA, WI |
| Quantity | 900 |
| UPC / GTIN / UDI-DI | 10885403108402 |
| Lot numbers | 0001304986 |
| Model numbers | PIG1280T |
Product
CareFusion Safe-T-Centesis Catheter Drainage Tray, Sterile, For Single Use Only, Rx only, Catalog Number PIG1280T, UDI Number 01)10885403108402(17) 210930(10)0001304986
Reason for recall
The 8 Fr catheter was manufactured with the 6.9 Fr needle instead of the 8 Fr needle.
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-1795-2020. 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.