Skip to content
Recall Observatory FDA recall evidence

Device product

PERIPHERAL BLOOD CULTURE DRAW, REF DYNDH1561

Z-0311-2024

November 01, 2023

Class II

Product summary

Firm
MEDLINE INDUSTRIES, LP - Northfield
Event
Event 93379
Status
Ongoing
Classification
Class II
Quantity
1770 kits
Official record key
device-enforcement:Z-0311-2024

Official wording

Reason: This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.

Code information: UDI/DI 40193489402811 (case), 10193489402810 (unit): Lot Numbers: 23EMF711, 23CMH027

Distribution pattern: US Nationwide distribution in the state of California.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.