ANESTHESIA TURNOVER KIT — Class II medical device recall Z-3072-2024
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-09-18, distributed in CA, IL, TX. A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non
| Recall number | Z-3072-2024 |
|---|---|
| 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 | 2024-06-18 |
| Classified | 2024-09-06 |
| Reported by FDA | 2024-09-18 |
| Distributed | CA, IL, TX |
| Quantity | 315 units |
| Reason classes | labeling, sterility |
| UPC / GTIN / UDI-DI | 10195327334208, 40195327334209 |
| Lot numbers | 23BBL312, 23CBE394, 23GBA457, 23GBA500, 23IBJ309 |
Product
ANESTHESIA TURNOVER KIT, Pack Number DYNJAA0377A
Reason for recall
A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes sterility during its use, there is an increased risk of patient infection.
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-3072-2024. 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.