Data Foundry

Medical device recalls 2024

1500ML SOFT LINER — Class II medical device recall Z-2696-2024

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 numberZ-2696-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated2024-03-22
Classified2024-08-22
Reported by FDA2024-08-28
DistributedNationwide (US)
Countries outside the USCA, CO, MX, OM, PA, QA, SG, SV
UPC / GTIN / UDI-DI10888277276222, 40888277276223
Lot numbers670220510, 670220607, 670220701, 670220721, 670220727, 670220825, 670220915, 670220928, 670221024, 670221115, 670221124, 670221202, 670221213, 670221220, 670221222, 670230206, 670230215, 670230331, 670230417, 670230508, 670230922, 670231019, 670231101, 670231116, 670231123, 670231205
Model numbersOR926K

Product

1500ML SOFT LINER, 1/4X6 TBG NS, REF OR926K

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-2696-2024. 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.