Cardinal Health Presource Packs Recall Over CliniClean Pericare Wipes Contamination (Ref. f1501f)
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 44 units of Presource Packs containing CliniClean Pericare Wipes 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.
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, medical-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
- KIT, CHONY ORTHO MAJOR SPINE, Catalog Number: POV2SCCPP, UDI-DI: 10198956285200 (each), 50198956285208 (case), Lot Number: NGKV3390
- KIT, ORTHOPLASTIC MICROVASCULAR, Catalog Number: PWVMFFABLI, UDI-DI: 10198956123915 (each), 50198956123913 (case), Lot Number: NGKT2394
44 units distributed to US Nationwide distribution.
What You Should Do
Consumers and healthcare providers should stop using the affected products.
Why This Matters
This Class II recall addresses potential localized skin irritation from contaminated wipes in urinary catheter trays distributed nationwide.
Source
FDA recall number Z-3105-2026, event ID 99553.
Original source: FDA Official Notice ↗
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Similar notices nationwide by 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 (990 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to September 15, 2026.
What People Ask
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