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
11 of 11 products
| Model / number | Product as published |
|---|---|
PBCGRGB28 | KIT, BLO ROBOTIC GYN |
PBVMLP22G | KIT , GYN MAJOR BARNES JEWIS |
PBVM0722D | KIT, GYN OPERATIVE LAPAROSCOPY |
PBV2MJMVH | KIT,MAJOR VAGINAL,PRESBYTERIAN |
PBV2MJMVH | KIT, GYN LAPAROSCOPY |
PB43LSEJG | KIT, GYN LAPAROSCOPY |
| — | GYNE ROBOTIC PACK CMC , Catalog Number: SMACGGRACE |
| — | LH GYN ROBOTICS PK , Catalog Number: SMAOCGYLHL |
| — | DAVINCI PACK WOMENS , Catalog Number: SMAVPDWTMC |
SMA4JGRODB | PK GYN ROBOTICS OD |
SMA4JLGODA | PK LAPAROSCOPY GYN OD |
- Lot codes and dates
21 of 21 products
Products covered by this recall # Barcodes Product as published 1 1019895612385450198956123852Lot Number: GKU1823 ; 2) PBVMLP22G, UDI-DI: 10198956123854(each), 50198956123852(case) 2 1019895612413450198956124132Lot Number: NGKU2052 ; 3) PBVM0722D, UDI-DI: 10198956124134(each), 50198956124132(case) 3 1019895612413450198956124132Lot Number: NGKU0856 ; 4) PBVM0722D, UDI-DI: 10198956124134(each), 50198956124132(case) 4 1019895612413450198956124132Lot Number: NGKU0957 ; 5) PBVM0722D, UDI-DI: 10198956124134(each), 50198956124132(case) 5 1019895612413450198956124132Lot Number: NGKU0856 ; 6) PBVM0722D, UDI-DI: 10198956124134(each), 50198956124132(case) 6 1019895628524850198956285246Lot Number: NGKU0957 ; 7) PBV2MJMVH, UDI-DI: 10198956285248(each), 50198956285246(case) 7 1019895612519350198956125191Lot Number: NGKV3390 ; 8) PB13GYAJD, UDI-DI: 10198956125193(each), 50198956125191(case) 8 1019895620099950198956200997Lot Number: NGKV3390 ; 9) PB43LSEJG, UDI-DI: 10198956200999(each), 50198956200997(case) 9 1019710682050650197106820504Lot Number: NGKW2883 ; 10) SMACGGRACE, UDI-DI: 10197106820506(each), 50197106820504(case) 10 1019710682050650197106820504Lot Number: NGKU0856 ; 11) SMACGGRACE, UDI-DI: 10197106820506(each), 50197106820504(case) 11 1019895625721450198956257212Lot Number: NGKU2052 ; 12) SMAOCGYLHL, UDI-DI: 10198956257214(each), 50198956257212(case) 12 1019895625721450198956257212Lot Number: NGKW0682 ; 13) SMAOCGYLHL, UDI-DI: 10198956257214(each), 50198956257212(case) 13 1019895625721450198956257212Lot Number: NGKW3769 ; 14) SMAOCGYLHL, UDI-DI: 10198956257214(each), 50198956257212(case) 14 1019895625721450198956257212Lot Number: NGKW3769 ; 15) SMAOCGYLHL, UDI-DI: 10198956257214(each), 50198956257212(case) 15 1019710667805350197106678051Lot Number: NGKW3769 ; 16) SMAVPDWTMC, UDI-DI: 10197106678053(each), 50197106678051(case) 16 1019710667805350197106678051Lot Number: GKU1823 ; 17) SMAVPDWTMC, UDI-DI: 10197106678053(each), 50197106678051(case) 17 1019710667054550197106670543Lot Number: GKU1823 ; 18) SMA4JGRODB, UDI-DI: 10197106670545(each), 50197106670543(case) 18 1019710667054550197106670543Lot Number: NGKU0129 ; 19) SMA4JGRODB, UDI-DI: 10197106670545(each), 50197106670543(case) 19 1019710667494950197106674947Lot Number: NGKU0129 ; 20) SMA4JLGODA, UDI-DI: 10197106674949(each), 50197106674947(case) 20 1019710667494950197106674947Lot Number: NGKU0129 ; 21) SMA4JLGODA, UDI-DI: 10197106674949(each), 50197106674947(case) - Amount recalled
- 1398 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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