Data Foundry

Medical device recalls 2024

MEDLINE Kits — Class I medical device recall Z-1095-2024

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-03-06, distributed nationwide. Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse

Recall numberZ-1095-2024
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated2023-11-15
Classified2024-02-24
Reported by FDA2024-03-06
DistributedNationwide (US)
Countries outside the USAE, CA, PA
Quantity385,028 units
Reason classessterility
UPC / GTIN / UDI-DI10195327196615, 10195327249113, 10889942561803, 10889942622580, 10889942778546, 40195327196616, 40195327249114, 40889942561804, 40889942622581, 40889942778547
Lot numbers21112457, 22022812, 22032993, 22094063, 22104208, 22CLA155, 22FBH338, 22FLA788, 22GLA774, 22IBG388, 22KLB047, 22OBE815, 23AME808, 23CLA672, 23CLA832, 23ELA032, 23EMI159, 23FLA055, 23FLA663, 23FME004, 23JMJ796
Model numbersCDS840228F, DYNDC2128B, DYNJ0352159C, DYNJ0352159D, DYNJ44087A

Product

MEDLINE Kits, trays, and packs labeled as follows: a) CATH LAB CDS, REF CDS840228F; b) PEDIATRIC PORT A CATH TRAY, REF DYNDC2128B; c) PK, RADIOLOGY, REF DYNJ44087A; d) PORT ACCESS PACK-LF, REF DYNJ0352159C; DYNJ0352159D

Reason for recall

Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.

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-1095-2024. 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.