The Recall Desk
ModerateFDA (Devices)·Z-3105-2026·Announced 2026-09-09

Cardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes

Cardinal Health is recalling 44 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall involves a potential contamination with a lubricant that may cause localized skin effects such as irritation or mild inflammation, which aligns with the criteria for low-risk contamination or minor labeling/quality errors.

Plain-English summary

Cardinal Health 200, LLC is recalling 44 units of Presource Packs containing CliniClean Pericare Wipes within BD Urinary Catheter Trays. The affected products are the KIT, CHONY ORTHO MAJOR SPINE (Catalog Number: POV2SCCPP) and the KIT, ORTHOPLASTIC MICROVASCULAR (Catalog Number: PWVMFFABLI). These items were distributed nationwide in the United States.

The recall was initiated because the CliniClean Pericare Wipes within the trays 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, including irritation, erythema, or mild inflammation.

Healthcare facilities and consumers should stop using these specific products immediately. Affected lots include Lot Number NGKV3390 (UDI-DI: 10198956285200) and Lot Number NGKT2394 (UDI-DI: 10198956123915). Users should contact Cardinal Health for further instructions on returning or disposing of the recalled items.

The recalled product

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
Affected units
44

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (8)

  • 1) POV2SCCPP
  • UDI-DI: 10198956285200(each)
  • 50198956285208(case)
  • Lot Number: NGKV3390
  • 2) PWVMFFABLI
  • UDI-DI: 10198956123915(each)
  • 50198956123913(case)
  • Lot Number: NGKT2394

Distribution

Distributed nationwide across the United States.