PlainRecalls
FDA Devices Moderate Class II Ongoing

Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: 1) BLOOD CULTURE KIT, REF DYNDH1462B; 2) BLOOD CULTURE KIT, REF DYNDH1622C; 3) BLOOD CULTR KT DIVRSN DEVICE, REF DYNDH1866.

Reported: July 30, 2025 Initiated: June 12, 2025 #Z-2155-2025

Product Description

Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: 1) BLOOD CULTURE KIT, REF DYNDH1462B; 2) BLOOD CULTURE KIT, REF DYNDH1622C; 3) BLOOD CULTR KT DIVRSN DEVICE, REF DYNDH1866.

Reason for Recall

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.

Details

Units Affected
15700 units
Distribution
Distributed domestically to California, Florida, Pennsylvania, and Texas. No international distribution.
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: 1) BLOOD CULTURE KIT, REF DYNDH1462B; 2) BLOOD CULTURE KIT, REF DYNDH1622C; 3) BLOOD CULTR KT DIVRSN DEVICE, REF DYNDH1866.. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 15700 units.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 30, 2025. Severity: Moderate. Recall number: Z-2155-2025.