FDA Recalls medium

Cardinal Health Presource Packs Recall Over CliniClean Pericare Wipes Contamination (Jul 29, 2026, 00:00 UTC)

Source: FDA · United States

Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.

Cardinal Health 200, LLC is recalling 956 units of Presource Packs containing CliniClean Pericare Wipes in BD Urinary Catheter Trays due to potential lubricant contamination.

Reading this FDA recall beyond the headline

This notice was issued by FDA on September 15, 2026 and geographically references United States. The FDA classifies this as a Class II recall, with the stated 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.", distributed us nationwide distribution.. FDA recall classes run from I (reasonable probability of serious harm) to III (unlikely to cause harm), so the class number is the fastest way to gauge severity here. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.

A quick skim tells you whether this affects you directly; a closer read tells you more. Check the scope, the source, and how recent the record is, then weigh it against related notices rather than treating any single one as a trend.

The original agency source is linked below so you can verify this record directly before acting on it. Its related labels are recall, product-safety, fda, medical-devices.

What Happened

Cardinal Health 200, LLC initiated a voluntary recall of Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays. The trays may contain wipes potentially contaminated with a lubricant used during the manufacturing process, which could cause localized skin effects including irritation, erythema, or mild inflammation if used on a patient.

Which Products Are Affected

The recall covers 956 units distributed nationwide in the United States. Affected products include:

  • KIT, ROBOTIC HYST, Catalog Number: PB41RHRM3, Lot Numbers: NGKU3049, NGKU4043
  • KIT, ROBOTIC HYST, Catalog Number: PB41RHRM4, Lot Number: NGKU4716
  • KIT, C SECTION, Catalog Number: PLVMCS22G, Lot Numbers: NGKU0957, NGKU0856, NGKU2052
  • KIT, C SECTION MARTIN, Catalog Number: PL22CSMMI, Lot Number: NGKU0129
  • KIT, C SECTION OREGON HEALTH, Catalog Number: PL57CS60N, Lot Number: NGKU2052
  • C SECTION PACK, Catalog Number: SMAHBCSECB, Lot Numbers: NGKU4716, 20251217
  • C SECTION PACK, Catalog Number: SMAHBCSEC3, Lot Number: NGKU2887 Additional catalog numbers listed include PL22CSM13. UDI-DI codes and case/each identifiers are provided in the recall notice. This is FDA Class II recall Z-3102-2026.

What You Should Do

Consumers and healthcare facilities should not use the affected products. Contact Cardinal Health 200, LLC for further instructions regarding returns or refunds.

Why This Matters

Use of potentially contaminated wipes may result in localized skin irritation, erythema, or mild inflammation.

Source

FDA recall Z-3102-2026, Cardinal Health 200, LLC, Waukegan, IL.

Original source: FDA Official Notice ↗

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Elsewhere in the country: similar length or severity timing 8

Beyond this FDA recall's own category, Areazine surfaces two nationwide peer sets: length-matched and severity/date-matched notices from elsewhere in the archive, distinct from the same-feed Related list above.

Similar body length

Nearest notices by article body length (1,611 characters here).

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Similar severity timing

Same severity (medium) notices issued closest in time to September 15, 2026.

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What People Ask

What people usually ask about a notice like this one.

What is this FDA recall about? ▾
Cardinal Health 200, LLC is recalling 956 units of Presource Packs containing CliniClean Pericare Wipes in BD Urinary Catheter Trays due to potential lubricant contamination.
Which agency issued this alert? ▾
This alert was issued by FDA. The original notice is available at the source link at the bottom of this article.
How is this recall classified, and why does that matter? ▾
The FDA classifies this as a Class II recall, citing "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." as the reason. Class I is the most serious (reasonable probability of serious harm), Class II is a moderate or temporary health risk, and Class III is unlikely to cause harm.
What area is affected? ▾
This alert affects United States. Check with FDA for the most current geographic scope.
Where can I find more FDA Recalls updates? ▾
Browse the full FDA Recalls feed on Areazine at areazine.com/recalls/fda/ for the latest updates from FDA and other agencies.

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