Skip to content

Medline Convenience Kits, containing BD ChloraPrep Clear -… recallZ-2154-2025 · MEDLINE INDUSTRIES, LP - Northfield · initiated Jun 12, 2025

Open, Classified

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from MEDLINE INDUSTRIES, LP - Northfield or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms for the patient.

FDA root cause category: Other

What the company is doing

On June 12, 2025, firm instructed customers to request stickers to over-label the affected convenience kits with a warning label indicating to remove the affected component and replace it with product from supply. No product is to be returned.

Recall details

Recall number
Z-2154-2025
Status
Open, Classified
Initiated by the company
Jun 12, 2025
Posted by the FDA
Jul 21, 2025
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Quantity
184 units
Product code
LRS
Distribution
Distributed domestically to California, Florida, Pennsylvania, and Texas. No international distribution.

Product description

Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: IV START KIT LAB DRAW-SH, REF CDS860014P

Code information (models, lots, serial numbers)

UDI/DI 10888277797819 (EA), 40888277797810 (CASE), Lot Numbers: 24EBR549

Devices named in this recall

1 device in the FDA device registry whose identifier appears in the recall's code information.

Other products in the same recall event

The FDA groups related products into one recall event (event 97154).

Sources and updates

How recalls are matched to devices · Editorial policy · Report an error on this page