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Cardinal Health Presource Packs Recall Over CliniClean Pericare Wipes Contamination (Ref. 1adab6)

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 2448 units of Presource Packs containing CliniClean Pericare Wipes within BD Urinary Catheter Trays due to potential lubricant contamination.

The full picture behind this FDA recall

This notice was issued by FDA on September 16, 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.

Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.

What Happened

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.

Which Products Are Affected

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays distributed nationwide in the United States. Affected catalog numbers include: PCVNCG540 (Lot NGKT3319), PCVNCG542 (Lot NGKU0951), PCVNCG55I (Lot NGKU0977), PVCGBOB10 (Lot NGKT2391), PVCGBOB11 (Lot NGKT2391), PVCGBOB12 (Lot NGKT2391), PVCGBOB17 (Lot NGKT2391), PVCGOHCOH (Lot NGKT2391), PVCGOHCPA (Lots NGKT3319, NGKU0951), PVHDCBAGK (Lot NGKT2391), PVHDCGVCP (Lots NGKV2393, NGKW2687), PVHDCGV40 (Lot NGKV2393), PVHDVAAGH (Lot NGKT2391), PVHDVPVCQ (Lots NGKV2393, NGKW2687), PVHDVPV43 (Lot NGKW2687), PVOCMGJ36 (Lot NGKT2391), PVOCOHNHE (Lots NGKT2391, NGKT2455), PVOCOH12O (Lot NGKT2391), PVVMCV07E (Lot NGKT2394), PVVMFP22R (Lot NGKT2394), PVVMFP245 (Lot NGKT2394), PVVMTH22J (Lots NGKU0856, NGKU0957), PVVMTO22R (Lot NGKT2394), PVVMTO241 (Lot NGKT2394), PVVMTO242 (Lot NGKT2394), PVVXTHLCG (Lot NGKT1789), PVV2CC10R (Lot NGKV3390), PVV2CC10S (Lots NGKV3390, NGKV2390), PVV2MJ01M (Lot NGKV3390), PVV207962 (Lot NGKT2391), PVV207963 (Lot NGKT2455), PVV207964 (Lot NGKT2391), PVV293340 (Lot NGKT2391), PVV293362 (Lot NGKT2391), PVV293363 (Lot NGKT2391), PVX4CAP14 (Lot NGKU1994), PVX4CRPR7 (Lot NGKU1994), PVX4THEAA (Lots NGKU4043, NGKU4716), PV15CGSPF (Lots NGKU0977, NGKU0951), PV15CGSPG (Lots NGKT3319, NGKU0951), PV15MJSPD (Lots NGKT3319, NGKU0977), PV24OHN29 (Lot NGKU0977), PV29OHMME (Lots NGKT3319, NGKU0977), PV3LOHSGJ (Lot NGKU1994), PV33TCMYB (Lot NGKU4716), PV33TCMY3 (Lot NGKU2887), PV40OHAR47 (Lot NGKT2391), PV40OHAR48 (Lots NGKT2391, NGKT2455), PV40OHAR49 (Lot NGKT2391), PV40OHJUD (Lots NGKT2455, NGKT2391), PV60OH15F (Lot NGKT2391), SCVCGPAACD (Lots NGKU0977, NGKU0951, NGKT3319), SCVCGTRACI, SCVCGVCG17 (Lot NGKU0957), SCVCGVCG18 (Lot NGKU0856), SCVCGVCS16 (Lots N/A, NGKV5078). Total of 2448 units. Recall number Z-3098-2026. Class II recall.

What You Should Do

Stop use of affected products. Contact Cardinal Health 200, LLC at 3651 Birchwood Dr, Waukegan, IL 60085-8337 for further instructions.

Why This Matters

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

Source

FDA recall Z-3098-2026, report date 20260909, Cardinal Health 200, LLC voluntary recall.

Original source: FDA Official Notice ↗

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Frequently Asked Questions

What people usually ask about a notice like this one.

What is this FDA recall about? ▾
Cardinal Health 200, LLC is recalling 2448 units of Presource Packs containing CliniClean Pericare Wipes within 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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