Kendall Spill Kit — Class II medical device recall Z-1082-2021
Terminated recall by Cardinal Health 200, LLC, reported 2021-02-17, distributed nationwide. Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreig
| Recall number | Z-1082-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cardinal Health 200, LLC, Waukegan, IL, United States |
| Recall initiated | 2021-01-07 |
| Classified | 2021-02-05 |
| Reported by FDA | 2021-02-17 |
| Terminated | 2024-02-14 |
| Distributed | Nationwide (US) |
| Quantity | 137,346 kits |
| Reason classes | foreign material |
| Lot numbers | 916197X, 916881X, 919683X, 920354X, 924620X, 928728X, 931205X |
Product
Kendall Spill Kit, 6 Per Case, NonsterileI, BB6016K
Reason for recall
Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
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-1082-2021. 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.