Data Foundry

Medical device recalls 2024

1 — Class II medical device recall Z-2697-2024

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-2697-2024
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
Quantity88,703 units
UPC / GTIN / UDI-DI40888277422279
Lot numbers670220512, 670220609, 670220621, 670220629, 670220712, 670220803, 670220815, 670220914, 670221009
Model numbersOR53926

Product

1,5L MED-SOFT LINER W/ 6MMX1,8M TUB. & ADULT VC, REF OR53926

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-2697-2024. 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.