Medline medical convenience kits labeled as: 1) TOTAL JOINT PACK… — Class II medical device recall Z-2791-2026

Ongoing recall by Medline Industries, LP, reported 2026-07-29, distributed in CT, FL, KS, MA, MD, MT, NY, OH…. Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL w

Recall number	`Z-2791-2026`
Product type	Medical device
Classification	Class II
Status	Ongoing
Voluntary or mandated	Voluntary
Recalling firm	Medline Industries, LP, Northfield, IL, United States
Recall initiated	2026-06-11
Classified	2026-07-23
Reported by FDA	2026-07-29
Distributed	CT, FL, KS, MA, MD, MT, NY, OH, OR, VA
Quantity	1,601 units
UPC / GTIN / UDI-DI	`10193489317183`, `10193489317244`, `10195327671723`, `10195327671808`, `10198459050671`, `10198459050688`, `10198459129889`, `10198459130977`, `10198459320491`, `40193489317184`, `40193489317245`, `40195327671724`, `40195327671809`, `40198459050672`, `40198459050689`, `40198459129880`, `40198459130978`, `40198459320492`
Lot numbers	`24KME109`, `24KMI926`, `24LBD222`, `24LBD661`, `24LBN441`, `24LBO744`, `24LMD416`, `25ABD265`, `25ABJ808`, `25ABL748`, `25ABM644`, `25ABP134`, `25BBS412`, `25BBT262`, `25BMB162`, `25BMI009`, `25CBD596`, `25CBO351`, `25CBO352`, `25DBC117`, `25DBE196`, `25DBS673`, `25DMB403`, `25DME458`, `25DMK347`, `25EBB260`, `25EBD582`, `25EBF179`, `25EBV317`, `25FBF363`, `25FBL400`, `25FBM835`, `25FBS372`, `25FMA695`, `25FMC143`

Product

Medline medical convenience kits labeled as: 1) TOTAL JOINT PACK Medline Kit SKU DYNJ65065A: 2) EXTREMITY/FOOT PACK Medline Kit SKU DYNJ65066B: 3) ANTERIOR CERVICAL-SMH Medline Kit SKU DYNJ907718B: 4) LAMINECTOMY-SMH Medline Kit SKU DYNJ907732C: 5) KYPHOPLASTY Medline Kit SKU DYNJ907984C: 6) LUMBAR LAMINECTOMY Medline Kit SKU DYNJ907987D: 7) KYPHOPLASTY TRAY Medline Kit SKU DYNJ908413C: 8) CRANIOTOMY Medline Kit SKU DYNJ910626: 9) NEURO SPINE Medline Kit SKU DYNJ910639.

Reason for recall

Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species.

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-2791-2026. 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.