Medline convenience kits containing semi-rigid suction liners labeled… — Class II medical device recall Z-3120-2024

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-09-18, distributed nationwide. XXX

Recall number	`Z-3120-2024`
Product type	Medical device
Classification	Class II
Status	Ongoing
Voluntary or mandated	Voluntary
Recalling firm	MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated	2024-06-27
Classified	2024-09-11
Reported by FDA	2024-09-18
Distributed	Nationwide (US)
Countries outside the US	CA, PA
Quantity	720 units
UPC / GTIN / UDI-DI	`10195327036966`, `10195327037147`, `10195327043216`, `10195327607104`, `40195327036967`, `40195327037148`, `40195327043217`, `40195327607105`
Lot numbers	`23LBD909`, `23LBF664`, `23LBS025`, `23LBS053`, `24ABY181`, `24ABY182`, `24CLA670`, `24CLA895`
Model numbers	`ARACT-30843`

Product

Medline convenience kits containing semi-rigid suction liners labeled as follows: a) AMB VITRECTOMY, Pack Number DYNJ59921B; b) AMB VITRECTOMY, Pack Number DYNJ59921BH; c) AMB OCULOPLASTICS MUSC, Pack Number DYNJ59923B; d) AMB OCULOPLASTICS MUSC, Pack Number DYNJ59923BH; e) AMB CUSTOM EYE, Pack Number DYNJ59924B; f) AMB CUSTOM EYE, Pack Number DYNJ59924BH; g) CATARACT-30843, Pack Number DYNJVB91139

Reason for recall

XXX

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-3120-2024. 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.