# Class II recall Z-0279-2027: Medline Industries, LP

**Predicate Speed & CAPA Advisory Opportunity Score:** 68/100

| Field | Value |
|---|---|
| Record | Device recall |
| Recall number | Z-0279-2027 |
| Recalling firm | Medline Industries, LP |
| Classification | Class II |
| Status | Ongoing |
| Voluntary / mandated | Voluntary: Firm initiated |
| Specialty | Other |
| Product | MEDLINE medical convenience kits labeled as:  TUBAL LIGATION RFD,  Medline Product Number/SKU DYNJ906291G |
| Reason | Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin. |
| Quantity | 3 kits |
| Distribution | Worldwide distribution - US Nationwide and the countries of CA, TC, AU, AE. |
| Recall initiated | 2026-09-09 |
| Reported | 2026-10-28 |
| Firm location | Northfield, IL, United States |

## Why this score
- Class II recall: usually triggers CAPA and quality-system remediation work.
- Recall is still ongoing.
- Posted 8 days ago.

Source: U.S. FDA openFDA (510(k) clearances and device enforcement reports) (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0279-2027%22). Last refreshed: 2026-11-04T21:30:53.898Z.
Data from the FDA openFDA API, which may lag official FDA databases. Informational only; not regulatory or legal advice.