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

20 of 20 products

Products covered by this recall
Model / numberProduct as published
KIT, GYN ROBOTIC GSAM , Catalog Number: PBCCGRSGD
PB35GYBJCKIT, GYN ROBOT ACCESSORY
PGVMOTBB19KIT, PRIMARY RESECTION
PGVM07C26KIT, LIVER TRANSPLANT SUPPORT
PGVM07C26KIT, LIVER TRANSPLANT SUPPORT
PGV2LTNHNKIT, LIVER TRANSPLANT SUPPORT
PG15OT92AKIT,UMMC GENERAL MAJOR TRANSPL
PG23MLNLDKIT,MAJOR LITHOTOMY NEW HAN
PG29GCPCKKIT, GENDER CARE
PG29GCPC3KIT, GENDER CARE
PG33LVMNCKIT, MUH LIVER
PG35HPBJKKIT, MIS HERNIA
PG43MJEJDKIT, GENERAL MAJOR
KIT, OPEN THORACOTOMY CMC , Catalog Number: PVCGOTACF
PVX4TAMYBKIT, MER THORACOTOMY ABDOMINAL
PVX4TAMYCKIT, MER THORACOTOMY ABDOMINAL
PV23HEVAEKIT, HEART II
PW35FABJEKIT, FLAP ACCESSORY
SBA23RBHNGHMC ROBOTIC PACK
SBA23RBHNHHMC ROBOTIC PACK
Lot codes and dates

32 of 32 products

Products covered by this recall
#BarcodesProduct as published
11019710637572350197106375721Lot Number: NGKU0957 ; 2) PB35GYBJC, UDI-DI: 10197106375723(each), 50197106375721(case)
21019895626411350198956264111Lot Number: NGKU2052 ; 3) PGVMOTBB19, UDI-DI: 10198956264113(each), 50198956264111(case)
31019895626443450198956264432Lot Number: NGKT2394 ; 4) PGVM07C26, UDI-DI: 10198956264434(each), 50198956264432(case)
41019895629289550198956292893Lot Number: NGKT2394 ; 5) PGVM07C27, UDI-DI: 10198956292895(each), 50198956292893(case)
51019895629249950198956292497Lot Number: NGKT2394 ; 6) PGV2LTNHN, UDI-DI: 10198956292499(each), 50198956292497(case)
61019895629249950198956292497Lot Number: NGKV2390 ; 7) PGV2LTNHN, UDI-DI: 10198956292499(each), 50198956292497(case)
71019710647504150197106475049Lot Number: NGKV3390 ; 8) PG15OT92A, UDI-DI: 10197106475041(each), 50197106475049(case)
81019895643202450198956432022Lot Number: NGKW2883 ; 9) PG23MLNLD, UDI-DI: 10198956432024(each), 50198956432022(case)
91019895629920750198956299205Lot Number: NGKU3969 ; 10) PG29GCPCK, UDI-DI: 10198956299207(each), 50198956299205(case)
101019895653249650198956532494Lot Number: NGKU4716 ; 11) PG29GCPC3, UDI-DI: 10198956532496(each), 50198956532494(case)
111019895618835850198956188356Lot Number: NGKU4716 ; 12) PG33LVMNC, UDI-DI: 10198956188358(each), 50198956188356(case)
121019895618835850198956188356Lot Number: NGKU1994 ; 13) PG33LVMNC, UDI-DI: 10198956188358(each), 50198956188356(case)
131019895618835850198956188356Lot Number: NGKU1994 ; 14) PG33LVMNC, UDI-DI: 10198956188358(each), 50198956188356(case)
141019895618835850198956188356Lot Number: NGKU1994 ; 15) PG33LVMNC, UDI-DI: 10198956188358(each), 50198956188356(case)
151019895612411050198956124118Lot Number: NGKU1994 ; 16) PG35HPBJK, UDI-DI: 10198956124110(each), 50198956124118(case)
161019895612411050198956124118Lot Number: NGKU0856 ; 17) PG35HPBJK, UDI-DI: 10198956124110(each), 50198956124118(case)
171019895612411050198956124118Lot Number: NGKU0957 ; 18) PG35HPBJK, UDI-DI: 10198956124110(each), 50198956124118(case)
181019895612411050198956124118Lot Number: NGKU0957 ; 19) PG35HPBJK, UDI-DI: 10198956124110(each), 50198956124118(case)
191019710659426150197106594269Lot Number: NGKU2052 ; 20) PG43MJEJD, UDI-DI: 10197106594261(each), 50197106594269(case)
201019710659426150197106594269Lot Number: NGKW2883 ; 21) PG43MJEJD, UDI-DI: 10197106594261(each), 50197106594269(case)
Amount recalled
846 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, 5:46 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.