Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-2588-2026Class II

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. MAJOR BASIN SET DYNJ85723

MEDLINE INDUSTRIES, LP - Northfield / initiated 2026-02-27 / Open, Classified / root cause: design

Medline Industries, LP began a recall of Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. MAJOR BASIN SET DYNJ85723 on . FDA classified it as Class II and gives the reason as "Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601". As of , the recall status on record is Open, Classified, and MDM tags the root cause as design.

Recall record

Recall number
Z-2588-2026
Classification
Class II
Status
Open, Classified
Initiated
Posted
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Product
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. MAJOR BASIN SET DYNJ85723
Product code
KDD Kit, Surgical Instrument, Disposable
Reason for recall
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Root cause tag
design
FDA root cause
No Marketing Application
Action
This entry catalogues SKUs communicated through the same letter documented in RES 98601 which were inadvertently missed in the initial report to the FDA. Firm began notifying customers on February 27, 2026 via letters titled "URGENT MEDICAL DEVICE RECALL". Customers were instructed to immediately check stock for affected product and quarantine any affected units. Upon receipt of the customers' response form reporting the quantity of affected product on hand, the firm will provide over-labels to place on affected inventory. Labels contain instructions for staff to remove and discard the affected component prior to using the kit.
Quantity in commerce
113,843 kits
Distribution
US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, FL, GA, IL, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, TN, TX, VA, WI, WY and the country of Barbados.
Product codes and lots
DYNJ85723 UDI-DI 10195327538491 Lot 24ABO130

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-2588-2026
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-2581-2026Class IIOngoingVoluntary: Firm initiated
Z-2582-2026Class IIOngoingVoluntary: Firm initiated
Z-2583-2026Class IIOngoingVoluntary: Firm initiated
Z-2584-2026Class IIOngoingVoluntary: Firm initiated
Z-2585-2026Class IIOngoingVoluntary: Firm initiated
Z-2586-2026Class IIOngoingVoluntary: Firm initiated
Z-2587-2026Class IIOngoingVoluntary: Firm initiated
Z-2588-2026Class IIOngoingVoluntary: Firm initiated
Z-2589-2026Class IIOngoingVoluntary: Firm initiated
Z-2590-2026Class IIOngoingVoluntary: Firm initiated
Z-2591-2026Class IIOngoingVoluntary: Firm initiated
Z-2592-2026Class IIOngoingVoluntary: Firm initiated
Z-2593-2026Class IIOngoingVoluntary: Firm initiated
Z-2594-2026Class IIOngoingVoluntary: Firm initiated
Z-2595-2026Class IIOngoingVoluntary: Firm initiated
Z-2596-2026Class IIOngoingVoluntary: Firm initiated