Medline Convenience Kits for Various Procedures: 1) CLOVIS RESP/INTUB… — Class II medical device recall Z-1183-2025
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2025-02-26, distributed in CA, NY. Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter du
| Recall number | Z-1183-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2025-01-09 |
| Classified | 2025-02-19 |
| Reported by FDA | 2025-02-26 |
| Distributed | CA, NY |
| Quantity | 0 kits |
| UPC / GTIN / UDI-DI | 10198459012235, 10198459012556, 40198459012236, 40198459012557 |
| Lot numbers | 24JDC400, 24KDA437 |
| Model numbers | ACC010809, ACC010813 |
Product
Medline Convenience Kits for Various Procedures: 1) CLOVIS RESP/INTUB DRAWER 2, Model Number ACC010809; 2) RESP/INTUBATION DRAWER #2, Model Number ACC010813
Reason for recall
Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.
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-1183-2025. 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.