Medline procedure kits labeled as: 1) CONTINUOUS BLOCK — Class I medical device recall Z-2442-2024
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-08-14, distributed nationwide. Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. L
| Recall number | Z-2442-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2024-04-08 |
| Classified | 2024-08-08 |
| Reported by FDA | 2024-08-14 |
| Distributed | Nationwide (US) |
| Quantity | 1,679,067 units |
| Reason classes | packaging, device malfunction |
| Lot numbers | 22EBD354, 22GLB081, 22HLA566, 22ILA092, 22JBO947, 22JLB162, 22LLA409, 22LLA800, 23BBO995, 23CBH823, 23CBH893, 23CBO440, 23DLA368, 23EBA854, 23EBC905, 23EBV028, 23FLA942, 23FLB123, 23GBE493, 23GLA313, 23GLA321, 23HBK783, 23HBO071, 23HBX547, 23HLA910, 23HLB303, 23ILA593, 23JBI435, 23JBN538, 23JBU321, 23KBJ159, 23LBC389, 23LBM602, 24ABQ693, 24ABQ696, 24ALA302, 24BBF612, 24BBH932, 24BBI322, 24BLA659 and 20 more |
Product
Medline procedure kits labeled as: 1) CONTINUOUS BLOCK, Pack Number DYNJRA0960C; 2) COMBINED SPINAL AND EPIDURAL, Pack Number DYNJRA1268C; 3) WAL- UNIVERSAL BLOCK TRAY, Pack Number DYNJRA1638C; 4) BASIC DIAGNOSTIC TRAY, Pack Number DYNJRA1928; 5) PREOP NERVE BLOCK TRAY, Pack Number DYNJRA2040; 6) UNIVERSAL BLOCK TRAY, Pack Number DYNJRA2097; 7) PAIN TRAY, Pack Number DYNJRA2230; 8) CONTINUOUS EPIDURAL, Pack Number PAIN1766A; 9) CONTINUOUS/CSE TRAY, Pack Number PAIN1856; 10) CONTINUOUS/CSE TRAY, Pack Number PAIN1856A; 11) 20G SINGLE DOSE EPIDURAL, Pack Number PAIN2047; 12) 20G SINGLE DOSE EPIDURAL/CHLOR, Pack Number PAIN2048
Reason for recall
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
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-2442-2024. 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.