Reported Sep 9, 2026 · Ongoing · Updated Sep 14, 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
| Model / number | Product as published |
|---|---|
| — | KIT, GYN ROBOTIC GSAM , Catalog Number: PBCCGRSGD |
PB35GYBJC | KIT, GYN ROBOT ACCESSORY |
PGVMOTBB19 | KIT, PRIMARY RESECTION |
PGVM07C26 | KIT, LIVER TRANSPLANT SUPPORT |
PGVM07C26 | KIT, LIVER TRANSPLANT SUPPORT |
PGV2LTNHN | KIT, LIVER TRANSPLANT SUPPORT |
PG15OT92A | KIT,UMMC GENERAL MAJOR TRANSPL |
PG23MLNLD | KIT,MAJOR LITHOTOMY NEW HAN |
PG29GCPCK | KIT, GENDER CARE |
PG29GCPC3 | KIT, GENDER CARE |
PG33LVMNC | KIT, MUH LIVER |
PG35HPBJK | KIT, MIS HERNIA |
PG43MJEJD | KIT, GENERAL MAJOR |
| — | KIT, OPEN THORACOTOMY CMC , Catalog Number: PVCGOTACF |
PVX4TAMYB | KIT, MER THORACOTOMY ABDOMINAL |
PVX4TAMYC | KIT, MER THORACOTOMY ABDOMINAL |
PV23HEVAE | KIT, HEART II |
PW35FABJE | KIT, FLAP ACCESSORY |
SBA23RBHNG | HMC ROBOTIC PACK |
SBA23RBHNH | HMC ROBOTIC PACK |
- Lot codes and dates
32 of 32 products
Products covered by this recall # Barcodes Product as published 1 1019710637572350197106375721Lot Number: NGKU0957 ; 2) PB35GYBJC, UDI-DI: 10197106375723(each), 50197106375721(case) 2 1019895626411350198956264111Lot Number: NGKU2052 ; 3) PGVMOTBB19, UDI-DI: 10198956264113(each), 50198956264111(case) 3 1019895626443450198956264432Lot Number: NGKT2394 ; 4) PGVM07C26, UDI-DI: 10198956264434(each), 50198956264432(case) 4 1019895629289550198956292893Lot Number: NGKT2394 ; 5) PGVM07C27, UDI-DI: 10198956292895(each), 50198956292893(case) 5 1019895629249950198956292497Lot Number: NGKT2394 ; 6) PGV2LTNHN, UDI-DI: 10198956292499(each), 50198956292497(case) 6 1019895629249950198956292497Lot Number: NGKV2390 ; 7) PGV2LTNHN, UDI-DI: 10198956292499(each), 50198956292497(case) 7 1019710647504150197106475049Lot Number: NGKV3390 ; 8) PG15OT92A, UDI-DI: 10197106475041(each), 50197106475049(case) 8 1019895643202450198956432022Lot Number: NGKW2883 ; 9) PG23MLNLD, UDI-DI: 10198956432024(each), 50198956432022(case) 9 1019895629920750198956299205Lot Number: NGKU3969 ; 10) PG29GCPCK, UDI-DI: 10198956299207(each), 50198956299205(case) 10 1019895653249650198956532494Lot Number: NGKU4716 ; 11) PG29GCPC3, UDI-DI: 10198956532496(each), 50198956532494(case) 11 1019895618835850198956188356Lot Number: NGKU4716 ; 12) PG33LVMNC, UDI-DI: 10198956188358(each), 50198956188356(case) 12 1019895618835850198956188356Lot Number: NGKU1994 ; 13) PG33LVMNC, UDI-DI: 10198956188358(each), 50198956188356(case) 13 1019895618835850198956188356Lot Number: NGKU1994 ; 14) PG33LVMNC, UDI-DI: 10198956188358(each), 50198956188356(case) 14 1019895618835850198956188356Lot Number: NGKU1994 ; 15) PG33LVMNC, UDI-DI: 10198956188358(each), 50198956188356(case) 15 1019895612411050198956124118Lot Number: NGKU1994 ; 16) PG35HPBJK, UDI-DI: 10198956124110(each), 50198956124118(case) 16 1019895612411050198956124118Lot Number: NGKU0856 ; 17) PG35HPBJK, UDI-DI: 10198956124110(each), 50198956124118(case) 17 1019895612411050198956124118Lot Number: NGKU0957 ; 18) PG35HPBJK, UDI-DI: 10198956124110(each), 50198956124118(case) 18 1019895612411050198956124118Lot Number: NGKU0957 ; 19) PG35HPBJK, UDI-DI: 10198956124110(each), 50198956124118(case) 19 1019710659426150197106594269Lot Number: NGKU2052 ; 20) PG43MJEJD, UDI-DI: 10197106594261(each), 50197106594269(case) 20 1019710659426150197106594269Lot 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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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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