Medline Kits — Class I medical device recall Z-1126-2024
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-1126-2024 |
|---|---|
| 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 | 5,724 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 00653160050226, 10193489460780, 10193489803860, 10193489916065, 10193489956573, 10195327031480, 10195327037253, 10195327059019, 10195327112554, 10195327152031, 10195327156374, 10195327279448, 10195327337254, 10195327382124, 10195327385521, 10195327407285, 10195327472603, 40193489460781, 40193489803861, 40193489916066, 40193489956574, 40195327031481, 40195327037254, 40195327059010, 40195327112555 and 9 more |
| Lot numbers | 22ABH632, 22ABW357, 22BBV644, 22CBF187, 22CBL660, 22CBV428, 22DBI589, 22EBE045, 22FBN595, 22FBO783, 22GBG399, 22GBL794, 22GBP859, 22GBZ358, 22HBA111, 22HBP383, 22IBF001, 22IBK002, 22IBS624, 22JBC220, 22JBQ351, 22KBN864, 22LBB812, 22LBH455, 22LMC016, 22LMH698, 22OBE478, 23ABG110, 23AME088, 23AMF669, 23BBR173, 23BMH365, 23CMB182, 23DBH202, 23DBI071, 23EBA347, 23EBG770, 23EBP259, 23EMA555, 23FBQ273 and 11 more |
| Model numbers | CDS983585G, CDS983916G, DYKM2222, DYNJ44917G, DYNJ44917I, DYNJ44917L, DYNJ47859C, DYNJ54869F, DYNJ64572A, DYNJ68875F, DYNJ68884B, DYNJ906183J, DYNJ906183K, EYP087W, LYN030KAGVD, LYN030POGVD, VAL011CTASD |
Product
Medline Kits, trays, and packs labeled as follows: a) CATARACT PACK, REF VAL011CTASD; b) CATARACT PACK, REF DYNJ68875F; c) CATARACT PACK, REF DYNJ54869F; d) CATARACT PREP PACK, REF DYNJ44917L; e) E-BLEPH CDS, REF CDS983585G; f) EYE CDS, REF CDS983916G; g) EYE KIT, REF DYKM2222; h) EYE PLASTIC PACK, REF DYNJ47859C; i) K PACK, REF LYN030KAGVD; j) OCULOPLASTY PACK, REF DYNJ64572A; k) OL OCULAR, REF DYNJ906183J; l) OL OCULAR, REF DYNJ906183K; m) P M CATARACT, REF DYNJ44917G; n) P M CATARACT, REF DYNJ44917I; o) P PACK, REF LYN030POGVD; p) R VITRECTOMY, REF EYP087W; q) VITRECTOMY PACK, REF DYNJ68884B
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-1126-2024. 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.