MEDLINE INDUSTRIES, LP Northfield FEMORAL ARTERY PACK-LF. Sterile Procedural Tray Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
FEMORAL ARTERY PACK-LF. Sterile Procedural Tray
Brand
MEDLINE INDUSTRIES, LP Northfield
Lot Codes / Batch Numbers
Item Number: DYNJ0826625Q, Case UDI/GTIN: 40193489377942, Unit UDI/GTIN: 10193489377941, Lot Number: 22KMA163, 22JME722
Products Sold
Item Number: DYNJ0826625Q, Case UDI/GTIN: 40193489377942, Unit UDI/GTIN: 10193489377941, Lot Number: 22KMA163, 22JME722
MEDLINE INDUSTRIES, LP Northfield is recalling FEMORAL ARTERY PACK-LF. Sterile Procedural Tray due to Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Recommended Action
Per FDA guidance
Medline Industries, LP notified consignees via email and first-class mail on 11/15/2022. Consignees were instructed to check stock for affected product and immediately quarantine. For any affected units, customers were instructed to over-label the sterile kits with a warning label indicating "Warning To Avoid Injury, Please Handle Blades with Care." No product is to be returned. Customers were also instructed to complete and return the response form and notify customers if further distributed.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026