Medline Industries, LP.

Agreement focuses on providing clinical solutions to support the Tohono O'odham Nation NORTHFIELD, Ill., Aug. 5, 2025 /PRNewswire/ -- Medline today announced a new Prime Vendor agreement with Arizona-based skilled nursing and assisted living provider, Tohono O'odham Nursing Care Authority (TONCA), which includes Archie Hendricks Skilled Nursing and Tohono O'odham Elder Assisted Living Residence. Continue Reading As part of the agreement, TONCA will source Medline's extensive portfolio of medical supplies, including its skin health products, programs, and clinical guidelines. The organization will also benefit from Medline's robust educational offerings and in-service support, delivered by a dedicated team of clinicians, skin health specialists, and product support specialists. "As TONCA's Prime Vendor, our goal is to help healthcare run better within their organization to meet their operational, clinical and financial goals," said Shannon Morelock, divisional manager, Medline Post-Acute Care. "TONCA approaches care with a compassionate mindset, and we look forward to supporting their staff with initiatives that help empower them in their daily care." Located in Sells, Arizona, an hour and 40 minutes outside Phoenix, TONCA is designed to empower elders to receive the care they need without leaving their Nation. "Medline is a natural partner for the Tohono O'odham Nursing Care Authority," said Ross Wilkoff, administrator at Tohono O'odham Nursing Care Authority. "When we seek collaborators, we look for a learning mindset, quality assurance embedded in workflows, and unwavering integrity. We look forward to leaning on Medline to help with staff education and processes that will drive measurable quality outcomes. We couldn't be more confident in our path forward—and we're counting on Medline to empower our future." Learn how Medline works with long-term care providers to improve clinical, financial and operational outcomes to help facilities thrive at . About Medline Medline is the largest provider of medical-surgical products and supply chain solutions serving all points of care. Through its broad product portfolio, resilient supply chain and leading clinical solutions, Medline helps healthcare providers improve their clinical, financial and operational outcomes. Headquartered in Northfield, Illinois, the company employs more than 43,000 people worldwide and operates in more than 100 countries and territories. To learn more about how Medline makes healthcare run better, visit . SOURCE Medline Industries, LP WANT YOUR COMPANY'S NEWS FEATURED ON PRNEWSWIRE.COM? 440k+ Newsrooms & Influencers 9k+ Digital Media Outlets 270k+ Journalists Opted In GET STARTED

The FDA said some recalled Codman perforators may have found their way into about 1,850 craniotomy kits from Medline. \n The FDA is amplifying an effort underway at medical device distributor Medline that aims to correct certain neurosurgery kits containing hardware that may cause bone drills to break apart during a craniotomy procedure.Previously, Integra LifeSciences launched a recall of some of its Codman disposable perforators due to an inadequate weld on the outer sleeve of the device. The company said the manufacturing defect may cause the 14mm perforator to disassemble, and, in some cases, prevent the device from automatically disengaging and stopping the drill’s rotation as designed.Earlier this month, the FDA said there have been 10 reported injuries but no deaths related to the issue—including complications from loose device fragments, plus skull and brain injuries, as well as the dangers in delaying the medical procedure itself. Integra’s Class I recall, first initiated in mid-April, spans more than 170,000 units. The company has directed healthcare providers to quarantine the affected products and return them for credit. The FDA said some of those recalled Codman perforators may have found their way into about 1,850 craniotomy kits from Medline, which also notified U.S. customers of the issue in April. This week, the agency spotlighted the distributor’s efforts to reach healthcare providers, which urged them to check their stock and affix warning labels that tell clinicians to remove the 14mm perforators before using the remainder of the kit.

This recall involves correcting certain devices and does not involve removing them from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it without correction. Affected Product Product Names: Medline Kits Containing Medtronic Aortic Root Cannula, labeled as follows: CABG OPNHRT SALEM HSP CARDIAC CABG CARDIAC PACK DR DANIELSON AC PACK HEART BASIN PACK-LF KARAS OH COMPONENT PACK OPEN HEART ADULT PART 1 CDS OPEN HEART B PACK-LF OPEN HEART PACK ZEESHAN OPEN HEART TOL DR RIORDAN PACK HEART BASIN PACK-LF CPB ADJUNCT PACK DR. CRESCENZO PACK PK CUST CV A&B CABRINI CO TOL DR RIORDAN PACK TOL DR. CRESCENZO PACK TOL DR. MORONT PACK Full List of Affected Devices Product Name UDI Lot Numbers CABG OPNHRT S HSP 10195327449650 23IBH906, 24EBC446, 24FMC989, 24GME639 CABG OPNHRT S HSP 10198459089503 24KMB217, 25AMG162 CARDIAC CABG 10195327490362 23LBV500, 24DBS178, 24EBK724, 24FBL825 CARDIAC PACK 10195327490355 24CBN830, 24DBS177 DR D AC PACK 10195327298258 23HBD834, 23IBF066 HEART BASIN PACK-LF 10195327047573 22GMD767, 22JMD290, 23GMC713, 23IMA561, 23KMC902 K OH COMPONENT PACK 10195327659684 24EBT996, 24IBR766, 24KBJ595, 24LBQ493 OPEN HEART ADULT PART 1 CDS 10195327034726 24CBG813 OPEN HEART B PACK-LF 10195327206383 22IMH938, 22KMC295, 23AMD800, 23DME198, 23GMD603, 23GMI093, 23HMG457, 23IMG457, 23KMJ484, 24AMG704, 24AMI684, 24BMG042, 24GMA506, 24GMA897 OPEN HEART PACK 10889942934164 23JBD049 Z OPEN HEART 10195327659882 24EBT606, 24IBE093, 24JBV568, 24KBR945 TOL DR R PACK 10195327166304 22GBL197, 22JBG283 TOL DR R PACK 10195327273484 23ABO787, 23EBT153, 23HBB950 TOL DR R PACK 10195327503390 24CBL126, 24EBV315, 24EBW136 HEART BASIN PACK-LF 10195327563561 24BMB798, 24DMH381, 24EMF949, 24GMF161, 24IMB237 TOL DR R PACK 10198459054242 24IBV027 TOL DR. C PACK 10195327176914 22HBX339 TOL DR. CRESCENZO PACK 10195327273750 22LBC389, 23EBQ439, 23HBG138 TOL DR. C PACK 10195327513818 23KBS878, 24CBB191, 24EBD828 TOL DR. C PACK 10198459054259 24FBO426, 24HBP282, 24JBL545, 24LBR173 TOL DR. M PACK 10195327513825 23KBC932, 24CBP602, 24EBV519 TOL DR. M PACK 10198459054266 24GBI558, 24GBX898, 24IBE173, 24IBE173A, 25ABG352 What to Do On February 21, 2025, Medline Industries, LP sent all affected customers an Immediate Action Required Medical Device Recall notice recommending the following actions: Complete the response form, listing all affected product in inventory. Complete the form even if there is no affected product in inventory. Once completed, customers will receive labels for affected inventory that instruct staff to remove the recalled component before using the kit. Notify any companies or individuals who may have received affected products. Reason for Correction Medline Industries LP is correcting certain lots of their medical procedure kits containing recalled Medtronic Aortic Root Cannulas due to the potential for excess material in the male luer. Medline is providing a sticker to attach to the procedure kits notifying the user not to use the aortic root cannula within the procedure kit and to use an aortic root cannula from another supplier. The use of the affected products may cause serious adverse health consequences, including procedure delay, neurological deficits/stroke (reversable and irreversible) and death. At this time, Medline Industries LP has reported no serious injuries or deaths related to this issue. Device Use Medline medical procedure kits containing Medtronic Aortic Root Cannulas are convenience kits used for various medical procedures. The Medtronic Aortic Root Cannula in the kit is used for six hours or less during surgery with the heart-and-lung machine (cardiopulmonary bypass). The cannula may also be used to remove air from the major artery (aorta) when a bypass procedure is finished. Contact Information Customers in the U.S. with questions about this recall should contact the Recall Department at 866-359-1704 or recalls@medline.com. Additional FDA Resources (listed in order of most to least recent): Unique Device Identifier (UDI) The unique device identifier (UDI) helps identify individual medical devices sold in the United States from distribution to use. The UDI allows for more accurate reporting, reviewing, and analyzing of adverse event reports so that devices can be identified more quickly, and as a result, problems potentially resolved more quickly. How do I report a problem? Health care professionals and consumers may report adverse reactions or quality problems they experienced using these devices to MedWatch: The FDA Safety Information and Adverse Event Reporting Program. Content current as of: 06/23/2025 Legal Disclaimer: EIN Presswire provides this news content "as is" without warranty of any kind. We do not accept any responsibility or liability for the accuracy, content, images, videos, licenses, completeness, legality, or reliability of the information contained in this article. If you have any complaints or copyright issues related to this article, kindly contact the author above.