ClearanceBrief
Recall Z-0119-2025 ยท LRO General Surgery Tray

MEDLINE INDUSTRIES, LP - Northfield

MEDLINE HEART CABG CDS, REF CDS983376R

DateOct 17, 2024 (initiated Aug 28, 2024)
StatusOpen, Classified
ReasonMedline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
Root causeUnder Investigation by firm
ActionMedline issued an UREGENT MEDICAL DEVICE NOTIFICATION to its consignees on 08/28/2024 via USPS first class mail and email. The notice explained the issue, potential risk, and requested the consignee quarantine the product and response to obtain labeling to be placed on the affected inventory. Distributors are directed to notify those to whom they shipped the affected product.
Quantity15 kits
DistributionUS Nationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K213481Medline General Surgery Tray
Medline Industries, Inc., May 24, 2022