Data Foundry

Medical device recalls 2025

Medline Sterile 0 — Class II medical device recall Z-1706-2025

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2025-05-07, distributed nationwide. It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking a

Recall numberZ-1706-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated2025-03-19
Classified2025-05-01
Reported by FDA2025-05-07
DistributedNationwide (US)
Countries outside the USCA, PA
Quantity2,519,991 units
Reason classessterility, packaging
UPC / GTIN / UDI-DI10884389338230, 10884389338247
Lot numbers23DJA038, 23DJA070, 23DJA114, 23EJA057, 23EJA128, 23EJA144, 23FJA110, 23GJA041, 23GJA118, 23GJA132, 23HJA033, 23IJA045, 23IJA052, 23IJA102, 23JJA103, 23JJA119, 23JJA144, 23LJA114, 24AJA025, 24AJA061, 24AJA180, 24BJA038, 24BJA092, 24BJA119, 24BJA158, 24CJA048, 24CJA117, 24CJA147, 24DJA010, 24HJA075, 24HJA178, 24KJA148
Model numbersRDI30296

Product

Medline Sterile 0.9% Normal Saline, USP, 100mL, REF RDI30296

Reason for recall

It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.

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-1706-2025. 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.