Centurion Kits — Class I medical device recall Z-1132-2024
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 number | Z-1132-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2023-11-15 |
| Classified | 2024-02-24 |
| Reported by FDA | 2024-03-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, CA, PA |
| Quantity | 14,234 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 00653160016840, 00653160050226, 00653160106022, 00653160193084, 00653160235906, 00653160290691, 00653160348361, 00653160349818, 00653160349887, 00653160350340, 00653160351491, 00653160352436, 00653160354096, 00653160356182, 00653160356199, 00653160357271, 10653160106029, 10653160193081, 10653160235903, 10653160290698, 10653160348368, 10653160349815, 10653160349884, 10653160350347, 10653160351498 and 7 more |
| Lot numbers | 023092190, 2022012480, 2022022350, 2022031750, 2022031790, 2022031850, 2022032850, 2022041180, 2022041280, 2022041880, 2022042580, 2022050980, 2022060290, 2022071180, 2022071280, 2022071390, 2022072890, 2022082280, 2022082980, 2022090690, 2022091390, 2022110490, 2022110890, 2022112290, 2022120290, 2022120790, 2022122090, 2022122890, 2023011690, 2023020690, 2023030390, 2023033090, 2023040390, 2023050390, 2023052290, 2023052490, 2023061290, 2023061390, 2023062690, 2023070390 and 6 more |
| Model numbers | CIT6180, DM640A, DM850A, DT18520A, DYNDC2817C, HT2375, ID1690, MNS12045A, MNS12995A, MNS13600, MNS3470, UT14785, UT19510, UT8565 |
Product
Centurion Kits, trays, and packs labeled as follows: a) BASIC PROCEDURE TRAY, REF MNS13600; b) BWH DAILY DRIVELINE MGMT KIT, REF DM640A; c) CIRCUMCISION TRAY, REF CIT6180; d) INCISION & DRAINAGE TRAY, REF ID1690; e) LACERATION TRAY, REF SUT19510; f) LACERATION TRAY, REF SUT19510; g) LACERATION TRAY, REF SUT8565; h) LACERATION TRAY, REF SUT8565; i) LINE REPAIR KIT, REF MNS12045A; j) MMC DAILY DRIVELINE MGMT KIT, REF DM850A; k) NEWBORN THORACOTOMY TRAY, REF MNS3470; l) NICU STERILE CENTRAL LINE CHANGE KIT, REF DT18520A; m) OMMAYA KITS - LATEX FREE, REF HT2375; n) PEDIATRIC ULTRASOUND KIT, REF MNS12995A; o) PORT ACCESS INFUSION KIT - 1IN NEEDLE, REF DYNDC2817C; p) WOUND CLOSURE AND IRRIGATION TRAY, REF SUT14785;
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-1132-2024. 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.