Medline medical procedure kits — Class I medical device recall Z-1456-2025

Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2025-04-16, distributed in CA, FL, MN, NY, OH, OR, PA, TX…. Medline medical procedure kits, containing Medtronic Aortic Root Cannula

Recall number	`Z-1456-2025`
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	2025-02-21
Classified	2025-04-04
Reported by FDA	2025-04-16
Distributed	CA, FL, MN, NY, OH, OR, PA, TX, WV
Quantity	1,310 units
UPC / GTIN / UDI-DI	`10195327034726`, `10195327047573`, `10195327206383`, `10195327298258`, `10195327449650`, `10195327490355`, `10195327490362`, `10195327659684`, `10195327659882`, `10198459089503`, `10889942934164`, `40195327034727`, `40195327047574`, `40195327206384`, `40195327298259`, `40195327449651`, `40195327490356`, `40195327490363`, `40195327659685`, `40195327659883`, `40198459089504`, `40889942934165`
Lot numbers	`22GMD767`, `22IMH938`, `22JMD290`, `22KMC295`, `23AMD800`, `23DME198`, `23GMC713`, `23GMD603`, `23GMI093`, `23HBD834`, `23HMG457`, `23IBF066`, `23IBH906`, `23IMA561`, `23IMG457`, `23JBD049`, `23KMC902`, `23KMJ484`, `23LBV500`, `24AMG704`, `24AMI684`, `24BMG042`, `24CBG813`, `24CBN830`, `24DBS177`, `24DBS178`, `24EBC446`, `24EBK724`, `24EBT606`, `24EBT996`, `24FBL825`, `24FMC989`, `24GMA506`, `24GMA897`, `24GME639`, `24IBE093`, `24IBR766`, `24JBV568`, `24KBJ595`, `24KBR945` and 3 more

Product

Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CABG OPNHRT S HSP, CARDIAC CABG, CARDIAC PACK, DR D AC PACK, HEART BASIN PACK-LF, K OH COMPONENT PACK, OPEN HEART ADULT PART 1 CDS, OPEN HEART B PACK-LF, OPEN HEART PACK, Z OPEN HEART.

Reason for recall

Medline medical procedure kits, containing Medtronic Aortic Root Cannula

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-1456-2025. 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.