Medline convenience kits containing semi-rigid suction liners labeled… — Class II medical device recall Z-3114-2024

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-09-18, distributed nationwide. Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500

Recall number	`Z-3114-2024`
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	3,117 units
UPC / GTIN / UDI-DI	`10193489708486`, `10195327236915`, `10195327464523`, `10195327464684`, `10195327507152`, `10195327507237`, `10195327512668`, `10195327549206`, `10195327549213`, `10195327615802`, `10195327618674`, `10195327641467`, `10198459012488`, `10889942002580`, `10889942440610`, `10889942777365`, `40193489708487`, `40195327236916`, `40195327464524`, `40195327464685`, `40195327507153`, `40195327507238`, `40195327512669`, `40195327549207`, `40195327549214` and 7 more
Lot numbers	`23LBE394`, `23LBF762`, `23LBH989`, `23LBT867`, `24ABU492`, `24ABV099`, `24ABV895`, `24ADB503`, `24BBA187`, `24BBB541`, `24BBK418`, `24BBK532`, `24CBC847`, `24CBD863`, `24CBE214`, `24CBG700`, `24CBI973`, `24CDA282`, `24CDB279`, `24DBA530`, `24DBH210`, `24DBH448`, `24DBI723`, `24DDB221`, `24DLA042`, `24DLA594`, `24EDA406`, `24FBA058`, `24FBC284`, `24FDA021`, `24FDA111`

Product

Medline convenience kits containing semi-rigid suction liners labeled as follows: a) ENDO KIT, Pack Number DYKE1092B; b) VIDEO BRONCHOSCOPY TRAY, Pack Number DYKE1666; c) SUCTION CANISTER KIT, Pack Number DYKM2196; d) SUCTION CANISTER KIT, Pack Number DYKM2196H; e) BRONCH LAB PACK-LF, Pack Number DYNJ24810B; f) THORACIC, Pack Number DYNJ907991F; g) RECTAL, Pack Number DYNJ908108A; h) ROBOTIC, Pack Number DYNJ908109C; i) CERVICAL, Pack Number DYNJ908748D; j) LAMI, Pack Number DYNJ908750D; k) MERCY TIFFIN BASIC-LF, Pack Number DYNJ909731; l) MERCY TIFFIN LITHOTOMY, Pack Number DYNJ909735; m) BASIC GENERAL SET UP, Pack Number DYNJ909945; n) BASIC GENERAL SET UP, Pack Number DYNJ909945A; o) AMB OCULOPLASTICS MUSC, Pack Number DYNJ910289; p) AMB OCULOPLASTICS MUSC, Pack Number DYNJ910289H; q) MTHZ TOTAL HIP, Pack Number DYNJC9311M; r) BRONCH KIT, Pack Number P906877

Reason for recall

Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.

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-3114-2024. 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.