FDA Recall Terminated

Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls, Ref. No. 2460-605

Recall: Z-0404-2022 · Initiated November 30, 2021

Recall

Recall Number
Z-0404-2022
Event Number
89150
Firm
MEDLINE INDUSTRIES, LP Northfield
FEI Number
1417592
Product Code
DIF
Status
Terminated
Root Cause
Storage
Initiated
November 30, 2021
Terminated
January 6, 2023
Address
3 Lakes Dr, Northfield, IL, 60093-2753

Description

Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls, Ref. No. 2460-605

Reason

Affected product was shipped from the warehouse at room temperature instead of the required refrigerated environment.

Action

The firm distributed an Urgent Recall Notification, dated 11/30/2021, to customers who purchased recalled product via first class mail. The notification informs customers that the firm is initiating a removal of Trilevel Serum Matrix Free from S-O2460605 kits due to product being compromised during shipment. Customers are instructed to immediately check their stock for affected product, quarantine any lot numbers associated with the recall, and destroy affected product. Customers were provided an Urgent Remedial Action Destruction Form to complete and return to the firm to indicate whether or not they possess recalled product and document product destruction. Completed forms are to be returned to the firm via email at [email protected] or by fax at 866-767-1290. If product was further distributed, customers are required to share the recall notification down the distribution chain. Customers with any questions about the recall are instructed to call 866-359-1704.

Distribution

US Nationwide distribution in the states of IL, OH, MS, and PA.

Quantity

14 units (individual)