FDA Recall Open, Classified

Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395

Recall: Z-1766-2025 · Initiated April 9, 2025

Recall

Recall Number
Z-1766-2025
Event Number
96732
Firm
MEDLINE INDUSTRIES, LP Northfield
FEI Number
1417592
Product Code
KDC
Status
Open, Classified
Root Cause
Under Investigation by firm
Initiated
April 9, 2025
Posted
May 15, 2025
Address
3 Lakes Dr, Northfield, IL, 60093-2753

Description

Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395

Reason

Three is the potential for the retractors to puncture through the sterile packaging.

Action

Medline issued a MEDLINE DEVICE RECALL notice to its consignees on 04/09/2025, The notice explained the issue, potential risk, and requested the following: REQUIRED ACTION: 1.Immediately check your stock for the affected item number(s) and the affected lot number(s) listed within the recall portal. Quarantine all affected product. Upon completion of the below actions, please 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 response form. Website link: https://recalls.medline.comRecall Reference #: R-25-072Recall Code: RECALL CODE 3.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. Please request that customers destroy any affected product. You should include your customers quantities on your response form. If you have any questions, contact the Recall Department at 866-359-1704 or [email protected].

Distribution

US Nationwide distribution.

Quantity

840 units