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

11 of 11 products

Products covered by this recall
Model / numberProduct as published
PBCGRGB28KIT, BLO ROBOTIC GYN
PBVMLP22GKIT , GYN MAJOR BARNES JEWIS
PBVM0722DKIT, GYN OPERATIVE LAPAROSCOPY
PBV2MJMVHKIT,MAJOR VAGINAL,PRESBYTERIAN
PBV2MJMVHKIT, GYN LAPAROSCOPY
PB43LSEJGKIT, GYN LAPAROSCOPY
GYNE ROBOTIC PACK CMC , Catalog Number: SMACGGRACE
LH GYN ROBOTICS PK , Catalog Number: SMAOCGYLHL
DAVINCI PACK WOMENS , Catalog Number: SMAVPDWTMC
SMA4JGRODBPK GYN ROBOTICS OD
SMA4JLGODAPK LAPAROSCOPY GYN OD
Lot codes and dates

21 of 21 products

Products covered by this recall
#BarcodesProduct as published
11019895612385450198956123852Lot Number: GKU1823 ; 2) PBVMLP22G, UDI-DI: 10198956123854(each), 50198956123852(case)
21019895612413450198956124132Lot Number: NGKU2052 ; 3) PBVM0722D, UDI-DI: 10198956124134(each), 50198956124132(case)
31019895612413450198956124132Lot Number: NGKU0856 ; 4) PBVM0722D, UDI-DI: 10198956124134(each), 50198956124132(case)
41019895612413450198956124132Lot Number: NGKU0957 ; 5) PBVM0722D, UDI-DI: 10198956124134(each), 50198956124132(case)
51019895612413450198956124132Lot Number: NGKU0856 ; 6) PBVM0722D, UDI-DI: 10198956124134(each), 50198956124132(case)
61019895628524850198956285246Lot Number: NGKU0957 ; 7) PBV2MJMVH, UDI-DI: 10198956285248(each), 50198956285246(case)
71019895612519350198956125191Lot Number: NGKV3390 ; 8) PB13GYAJD, UDI-DI: 10198956125193(each), 50198956125191(case)
81019895620099950198956200997Lot Number: NGKV3390 ; 9) PB43LSEJG, UDI-DI: 10198956200999(each), 50198956200997(case)
91019710682050650197106820504Lot Number: NGKW2883 ; 10) SMACGGRACE, UDI-DI: 10197106820506(each), 50197106820504(case)
101019710682050650197106820504Lot Number: NGKU0856 ; 11) SMACGGRACE, UDI-DI: 10197106820506(each), 50197106820504(case)
111019895625721450198956257212Lot Number: NGKU2052 ; 12) SMAOCGYLHL, UDI-DI: 10198956257214(each), 50198956257212(case)
121019895625721450198956257212Lot Number: NGKW0682 ; 13) SMAOCGYLHL, UDI-DI: 10198956257214(each), 50198956257212(case)
131019895625721450198956257212Lot Number: NGKW3769 ; 14) SMAOCGYLHL, UDI-DI: 10198956257214(each), 50198956257212(case)
141019895625721450198956257212Lot Number: NGKW3769 ; 15) SMAOCGYLHL, UDI-DI: 10198956257214(each), 50198956257212(case)
151019710667805350197106678051Lot Number: NGKW3769 ; 16) SMAVPDWTMC, UDI-DI: 10197106678053(each), 50197106678051(case)
161019710667805350197106678051Lot Number: GKU1823 ; 17) SMAVPDWTMC, UDI-DI: 10197106678053(each), 50197106678051(case)
171019710667054550197106670543Lot Number: GKU1823 ; 18) SMA4JGRODB, UDI-DI: 10197106670545(each), 50197106670543(case)
181019710667054550197106670543Lot Number: NGKU0129 ; 19) SMA4JGRODB, UDI-DI: 10197106670545(each), 50197106670543(case)
191019710667494950197106674947Lot Number: NGKU0129 ; 20) SMA4JLGODA, UDI-DI: 10197106674949(each), 50197106674947(case)
201019710667494950197106674947Lot 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.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Cardinal Health 200, LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (weekly enforcement report) notice

Data as of Sep 19, 7:08 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.