FDA Enforcement Class II Ongoing

MEDLINE BLOOD CLUTURE KIT, Reorder #: DYNDH1592

Recall: Z-0122-2023 · Reported November 2, 2022

Enforcement

Recall Number
Z-0122-2023
Event ID
90911
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
MEDLINE INDUSTRIES, LP - Northfield
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Other
Report Date
November 2, 2022
Initiation Date
September 9, 2022
Classification Date
October 21, 2022
Address
3 Lakes Dr, N/A, Northfield, IL, 60093-2753, United States

Description

MEDLINE BLOOD CLUTURE KIT, Reorder #: DYNDH1592

Reason

Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an expiration date that does not match the date listed on the kit.

Code Info

UDI/DI (01)40193489497220 (case), (01)10193489497229 (kit), Lot Numbers: 22GME974, 22FMF309

Distribution

US Nationwide distribution in the state of California.

Quantity

1600 kits