Reported Sep 9, 2026 · Ongoing · Updated Sep 16, 2026

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays

Cardinal Health 200, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Cardinal Health 200, LLC · 3651 Birchwood Dr · Waukegan, IL · 60085-8337

Is this the product you have?

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays

56 of 56 products

Products covered by this recall
Model / numberProduct as published
PCVNCG540KIT, GVI OPEN HEART A B
PCVNCG542KIT, GVI OPEN HEART A B
PCVNCG55IKIT, GVI OPEN HEART A B
PVCGBOB10KIT, BLO BASIC OPEN HEART
PVCGBOB10KIT, BLO BASIC OPEN HEART
PVCGBOB12KIT, BLO BASIC OPEN HEART
PVCGBOB17KIT, BLO BASIC OPEN HEART
KIT, OPEN HEART CON , Catalog Number: PVCGOHCOH
KIT,OPEN HEART ADULT MDST , Catalog Number: PVCGOHCPA
KIT, CABG , Catalog Number: PVHDCBAGK
KIT, ORP CABG , Catalog Number: PVHDCGVCP
PVHDCGV40KIT, ORP CABG
KIT, VALVE , Catalog Number: PVHDVAAGH
KIT, ORP VALVE , Catalog Number: PVHDVPVCQ
PVHDVPV43KIT, ORP VALVE
PVOCMGJ36KIT, MAJOR CARDIAC
KIT, OPEN HEART DH , Catalog Number: PVOCOHNHE
PVOCOH12OKIT, OPEN HEART
PVVMCV07EKIT, CAROTID ENDARTERECTOMY
PVVMFP22RKIT, FEM POP BARNES JEW
Lot codes and dates

83 of 83 products

Products covered by this recall
#BarcodesProduct as published
11019895631246350198956312461Lot Number: NGKT3319 ; 2) PCVNCG542, UDI-DI: 10198956312463(each), 50198956312461(case)
21019710628305950197106283057Lot Number: NGKU0951 ; 3) PCVNCG55I, UDI-DI: 10197106283059(each), 50197106283057(case)
31019895621988550198956219883Lot Number: NGKU0977 ; 4) PVCGBOB10, UDI-DI: 10198956219885(each), 50198956219883(case)
41019895622067650198956220674Lot Number: NGKT2391 ; 5) PVCGBOB11, UDI-DI: 10198956220676(each), 50198956220674(case)
51019895625647750198956256475Lot Number: NGKT2391 ; 6) PVCGBOB12, UDI-DI: 10198956256477(each), 50198956256475(case)
61019895639338750198956393385Lot Number: NGKT2391 ; 7) PVCGBOB17, UDI-DI: 10198956393387(each), 50198956393385(case)
71019895602227050198956022278Lot Number: NGKT2391 ; 8) PVCGOHCOH, UDI-DI: 10198956022270(each), 50198956022278(case)
81019710666677750197106666775Lot Number: NGKT2391 ; 9) PVCGOHCPA, UDI-DI: 10197106666777(each), 50197106666775(case)
91019710666677750197106666775Lot Number: NGKT3319 ; 10) PVCGOHCPA, UDI-DI: 10197106666777(each), 50197106666775(case)
101019710666677750197106666775Lot Number: NGKT3319 ; 11) PVCGOHCPA, UDI-DI: 10197106666777(each), 50197106666775(case)
111019710694647350197106946471Lot Number: NGKU0951 ; 12) PVHDCBAGK, UDI-DI: 10197106946473(each), 50197106946471(case)
121019710694647350197106946471Lot Number: NGKT2391 ; 13) PVHDCBAGK, UDI-DI: 10197106946473(each), 50197106946471(case)
131019710694647350197106946471Lot Number: NGKT2391 ; 14) PVHDCBAGK, UDI-DI: 10197106946473(each), 50197106946471(case)
141019895625459650198956254594Lot Number: NGKT2391 ; 15) PVHDCGVCP, UDI-DI: 10198956254596(each), 50198956254594(case)
151019895625459650198956254594Lot Number: NGKV2393 ; 16) PVHDCGVCP, UDI-DI: 10198956254596(each), 50198956254594(case)
161019895625459650198956254594Lot Number: NGKV2393 ; 17) PVHDCGVCP, UDI-DI: 10198956254596(each), 50198956254594(case)
171019895625459650198956254594Lot Number: NGKW2687 ; 18) PVHDCGVCP, UDI-DI: 10198956254596(each), 50198956254594(case)
181019895625459650198956254594Lot Number: NGKV2393 ; 19) PVHDCGVCP, UDI-DI: 10198956254596(each), 50198956254594(case)
191019895632694150198956326949Lot Number: NGKV2393 ; 20) PVHDCGV40, UDI-DI: 10198956326941(each), 50198956326949(case)
201019710694645950197106946457Lot Number: NGKV2393 ; 21) PVHDVAAGH, UDI-DI: 10197106946459(each), 50197106946457(case)
Amount recalled
2448 units

This recall covers 12 products

The agency filed one notice per product. You are reading one of them; the other 11 are below.

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Data as of Sep 19, 7:10 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.