DeviceSignal · Recall classified

Cardinal Health 200, LLC

FDA classified a device recall on 2026-09-03 · Class II · Z-3105-2026

EventRecall classified
Effective2026-09-03
ClassificationClass II

On 2026-09-03 the FDA classified a device recall from Cardinal Health 200, LLC as Class II. Product: Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays…. Recall Z-3105-2026. The firm initiated it on 2026-07-29. This reports the classification FDA published on that date.

Reported facts

Recall number
Z-3105-2026
Classification
Class II
Classified on
2026-09-03
Initiated on
2026-07-29
Firm
Cardinal Health 200, LLC
Reason
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, CHONY ORTHO MAJOR SPINE , Catalog Number: POV2SCCPP; 2) KIT,ORTHOPLASTIC MICROVASCULAR, Catalog Number: PWVMFFABLI

Every field above is as fda_device_enforcement published it. Nothing on this page is our interpretation.

Provenance

Source
fda_device_enforcement
Source record
Z-3105-2026
Snapshot hash
2ad9ab6cbee6c5eb2f0d4298731a8c9755893d917528d78bf00a015fa69a0494
Source URL
https://download.open.fda.gov/device/enforcement/device-enforcement-0001-of-0001.json.zip
Observed
2026-09-15T12:38:10.708Z
Transform
fda_device_enforcement_to_recall v1
Event rule
fda_device_recall_classified v1
Event key
64ac1b5367bc9b34f9e65c6e1f846f02e6fb549478a112bf442598eda8f65a54
Signal type
device_recall.classified

Source terms that apply

More DeviceSignal signals What DeviceSignal is

Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)