MEDLINE INDUSTRIES, LP Northfield MEDLINE LINQ TRAY, REF DYNJ65880A. Convenience kit used in medical/surgical procedures. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MEDLINE LINQ TRAY, REF DYNJ65880A. Convenience kit used in medical/surgical procedures.
Brand
MEDLINE INDUSTRIES, LP Northfield
Lot Codes / Batch Numbers
GTIN (01) 40195327002535, Lot Number 22DBJ856
Products Sold
GTIN (01) 40195327002535, Lot Number 22DBJ856
MEDLINE INDUSTRIES, LP Northfield is recalling MEDLINE LINQ TRAY, REF DYNJ65880A. Convenience kit used in medical/surgical procedures. due to Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
Recommended Action
Per FDA guidance
Medline disseminated MEDICAL DEVICE RECALL notice by US mail on 09/30/2022, The notices explained the issue and requested the following: "REQUIRED ACTION: 1.Immediately check your stock for the affected item number and the affected lot numbers listed on the recall portal. Destroy affected product. 2.Please use the link and the information below to complete your response form. Please list the quantity of affected product you have in inventory on the form. Even if you do not have any affected product in inventory, please complete and submit the form. The login for completing the response form is: Website link: https://recalls.medline.com Recall Reference #: R-22-149-FG Recall Code: RXXXXXXX 3.Upon completion of the form, please destroy affected product. Your account will receive credit once the response form is submitted. 4.If you are a distributor, or have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. Have the customers document and destroy any affected product. You should include your customers quantities on your response form. If you have any questions, please contact the Recall Department at 866-359-1704."
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