Data Foundry

Medical device recalls 2024

MEDLINE 4 — Class II medical device recall Z-1454-2024

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-04-10, distributed nationwide. Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The

Recall numberZ-1454-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated2024-02-23
Classified2024-03-29
Reported by FDA2024-04-10
DistributedNationwide (US)
Countries outside the USCA, PA
Quantity800 units
Reason classessterility, packaging
UPC / GTIN / UDI-DI10884389097359, 40884389097350
Lot numbers2023031390

Product

MEDLINE 4.5 IN WIRE CUT SCISSORS, Product Code DYND04006

Reason for recall

Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

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-1454-2024. 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.