Medline medical procedure kits labeled as follows: a) HEART… — Class II medical device recall Z-2701-2024
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-08-28, distributed nationwide. A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
| Recall number | Z-2701-2024 |
|---|---|
| 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 | 2024-03-22 |
| Classified | 2024-08-22 |
| Reported by FDA | 2024-08-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CO, MX, OM, PA, QA, SG, SV |
| Quantity | 26,096 units |
| UPC / GTIN / UDI-DI | 10193489214277, 10193489308099, 10193489968040, 10195327226992, 10195327330026, 10195327487942, 10195327488611, 10195327505851, 40193489214278, 40193489308090, 40193489968041, 40195327226993, 40195327330027, 40195327487943, 40195327488612, 40195327505852 |
| Lot numbers | 22EBC373, 22EBD234, 22EBE775, 22EBF837, 22FBV877, 22FDA441, 22FMB396, 22FMG767, 22GBT729, 22GDA574, 22IBA627, 22IMB116, 22JBE922, 22JBP917, 22JDB543, 22KBJ447, 22LDB596, 22LMA842, 23ABA707, 23ADB285, 23AMI823, 23BBB611, 23BBI384, 23CBB846, 23CBC455, 23CBK197, 23DBK952, 23EBF908, 23FBD020, 23FBG375, 23FBJ258, 23FBO404, 23FBV764, 23FBV848, 23GBO428, 23GBO470, 23GBW761, 23GMH322, 23HBA337, 23HBC022 and 22 more |
| Model numbers | DYKE1872A, DYKE1921A, DYKE1922A, DYNJ901681D, DYNJ902387K, DYNJ902752C, DYNJ905515D, DYNJS2035C |
Product
Medline medical procedure kits labeled as follows: a) HEART ANESTHESIA SET UP, REF DYNJ902752C, b) KIT ENDO, REF DYKE1872A, c) LOWER ENDO KIT, REF DYKE1921A, d) PACEMAKER, REF DYNJ901681D, e) UPPER ENDO KIT, REF DYKE1922A, f) VASCULAR, REF DYNJ905515D, g) VASCUALR, REF DYNJ902387K, h) VASCULAR III, REF DYNJS2035C
Reason for recall
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
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-2701-2024. 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.