Medline convenience kits containing semi-rigid suction liners labeled… — Class II medical device recall Z-3121-2024

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-3121-2024`
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	1,076 units
UPC / GTIN / UDI-DI	`10193489951592`, `10195327072612`, `10195327195434`, `10195327219673`, `10195327464707`, `10195327464738`, `10195327464752`, `10195327464776`, `10195327507022`, `10195327507039`, `10195327507077`, `10195327507107`, `10195327507169`, `10195327507183`, `10195327507190`, `10195327507244`, `10195327568382`, `10195327635336`, `10195327639280`, `10195327639303`, `10195327639341`, `10195327654535`, `40193489951593`, `40195327072613`, `40195327195435` and 19 more
Lot numbers	`23LBS081`, `23LBT897`, `23LBU932`, `23LBV779`, `23LDB386`, `23LDB793`, `23LMC113`, `24ABA222`, `24ABL204`, `24ABO437`, `24ABS361`, `24ABT063`, `24ABW989`, `24ABY029`, `24AME301`, `24AMJ018`, `24BBI407`, `24BBK598`, `24BBS375`, `24CBA353`, `24CBC838`, `24CBE409`, `24CBH612`, `24CBK626`, `24CBM378`, `24CBO655`, `24CBO720`, `24CBP714`, `24CBU878`, `24CDC175`, `24CMH075`, `24DBC165`, `24DDB322`, `24EBH235`, `24EBH236`, `24EDA091`, `24FBA023`, `4EBH232`

Product

Medline convenience kits containing semi-rigid suction liners labeled as follows: a) LAMINECTOMY CDS, Pack Number CDS981510L; b) ORTHO TRAUMA-LF, Pack Number DYNJ900720D; c) ORTHO TRAUMA-LF, Pack Number DYNJ900720F; d) KNEE ARTHROSCOPY, Pack Number DYNJ908090C; e) LAMINECTOMY, Pack Number DYNJ908091B; f) PODIATRY, Pack Number DYNJ908092C; g) ANTERIOR TOTAL HIP, Pack Number DYNJ908095B; h) CRANI, Pack Number DYNJ908097A; i) HIP PINNING, Pack Number DYNJ908102B; j) (76) LOWER EXTREMITY, Pack Number DYNJ908103B; k) SHOULDER ARTHROSCOPY, Pack Number DYNJ908110B; m) HAND-LF, Pack Number DYNJ908425; n) TOTAL JOINT, Pack Number DYNJ908660A; o) MERCY TIFFIN HAND, Pack Number DYNJ909734; p) MERCY TIFFIN TOTAL KNEE, Pack Number DYNJ909738; q) MTHZ KNEE ARTHROSCOPY, Pack Number DYNJ909740; r) ACL-WHSC, Pack Number DYNJ910074A; s) EXTREMITY-WHSC, Pack Number DYNJ910077; t) EXTREMITY-WHSC, Pack Number DYNJ910077A; u) KNEE ARTHROSCOPY-WHSC, Pack Number DYNJ910080A; v) MICRODISC, Pack Number DYNJ910370; w) MTHZ TOTAL HIP, Pack Number DYNJC9311L

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-3121-2024. 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.