FDA Device recall Z-1082-2021
Kendall Spill Kit, 6 Per Case, NonsterileI, BB6016K
- FDA Device
- Class II
- terminated
- Published 2021-02-17
On 2021-02-17 the FDA classified a Class II recall of Kendall Spill Kit, 6 Per Case, NonsterileI, BB6016K by Cardinal Health 200, citing gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1082-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-01-07 |
| Published | 2021-02-17 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Cardinal Health 200 |
| Distribution | US |
Product
Kendall Spill Kit, 6 Per Case, NonsterileI, BB6016K
Reason
Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
Identifiers
| code_info | Lots: 916197X 916881X 919683X 920354X 924620X 928728X 931205X |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1082-2021%22
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