ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage:… — Class II medical device recall Z-1284-2019
Terminated recall by Cardinal Health 200, LLC, reported 2019-05-15, distributed nationwide. Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rub
| Recall number | Z-1284-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cardinal Health 200, LLC, Mansfield, MA, United States |
| Recall initiated | 2019-03-22 |
| Classified | 2019-05-06 |
| Reported by FDA | 2019-05-15 |
| Terminated | 2021-08-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | BS, CA, CL, IL, JP |
| Quantity | 21,082 |
| Reason classes | labeling |
| Lot numbers | 708265X, 709766X, 712108X, 713853X, 719505X, 723645X, 726111X, 727029X, 730304X, 735321X, 803307X, 803990X, 808097X, 809318X, 812914X, 815537X, 821910X, 825016X, 826407X, 833752X |
Product
ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
Reason for recall
Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rubber latex in the goggle strap
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-1284-2019. 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.