MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2022 - (Recall #: Z-0121-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

MEDLINE PHERIPHERAL BLOOD CULTURE DRAW, Reorder #: DYNDH1561

Product Classification:

Class II

Date Initiated: September 9, 2022

Date Posted: November 2, 2022

Recall Number: Z-0121-2023

Event ID: 90911

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 1020 kits

Code Information:

UDI/DI: (01)40193489402811 (case), (01)10193489402810 (kit), Lot Number 22FMF307

Distribution Pattern:

US Nationwide distribution in the state of California.

Voluntary or Mandated:

Voluntary: Firm initiated