MEDLINE Medical Procedure Kits labeled as: recall status
⚠ Recall found. MEDLINE Medical Procedure Kits labeled as is named in 20 official recalls in our current data. Details and the official notices are below — act on the remedy in the official notice.
- Brand
- Medline Industries
Recalls naming this model
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2485-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2486-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2488-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2489-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2490-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2491-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2492-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2493-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2494-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2495-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2496-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2498-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2499-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2500-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2501-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2502-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2504-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2506-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2507-2026 ·
Official record ↗
FDA Class II · Medical device · June 24, 2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Official ID Z-2508-2026 ·
Official record ↗
See all Medline Industries recalls →
Compiled from official public-domain CPSC, NHTSA, and FDA data. Sources last checked July 24, 2026 at 1:09 AM UTC.