MEDLINE PEDI ELBOW CLOSED SUCTION CATHETER — Class II medical device recall Z-0112-2018
Terminated recall by Medline Industries Inc, reported 2017-11-29, distributed in FL, GA, IN, MD, NJ, TN, UT. Products labeled as sterile were distributed prior to sterilization
| Recall number | Z-0112-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries Inc, Northfield, IL, United States |
| Recall initiated | 2017-10-10 |
| Classified | 2017-11-18 |
| Reported by FDA | 2017-11-29 |
| Terminated | 2020-08-04 |
| Distributed | FL, GA, IN, MD, NJ, TN, UT |
| Countries outside the US | HN, NI |
| Quantity | 190 units |
| Reason classes | labeling, sterility |
| Lot numbers | 2861707008 |
| Model numbers | DYNCPE8 |
Product
MEDLINE PEDI ELBOW CLOSED SUCTION CATHETER, 8Fr, REF DYNCPE8
Reason for recall
Products labeled as sterile were distributed prior to sterilization
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-0112-2018. 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.