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FDA (Device enforcement)Recalled 2026-07-29class ii

Cardinal Health 200, LLC: Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, GYN ROBOTIC GSAM , Catalog Number: PBCCGRSGD; 2) KIT, GYN ROBOT ACCESSORY , Cat

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Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, GYN ROBOTIC GSAM , Catalog Number: PBCCGRSGD; 2) KIT, GYN ROBOT ACCESSORY , Catalog Number: PB35GYBJC; 3) KIT, PRIMARY RESECTION , Catalog Number: PGVMOTBB19; 4) KIT, LIVER TRANSPLANT SUPPORT , Catalog Num

  • UPC 10197106840085
  • UPC 50197106840083
  • UPC 10197106375723
  • UPC 50197106375721
  • UPC 10198956264113
  • UPC 50198956264111
  • UPC 10198956264434
  • UPC 50198956264432
  • UPC 10198956292895
  • UPC 50198956292893
  • UPC 10198956292499
  • UPC 50198956292497
  • UPC 10197106475041
  • UPC 50197106475049
  • UPC 10198956432024
  • UPC 50198956432022
  • UPC 10198956299207
  • UPC 50198956299205
  • UPC 10198956532496
  • UPC 50198956532494
  • UPC 10198956188358
  • UPC 50198956188356
  • UPC 10198956124110
  • UPC 50198956124118
  • UPC 10197106594261
  • UPC 50197106594269
  • UPC 10195594816469
  • UPC 50195594816467
  • UPC 10197106892404
  • UPC 50197106892402
  • UPC 10198956329379
  • UPC 50198956329377
  • UPC 10198956062160
  • UPC 50198956062168
  • UPC 10198956142282
  • UPC 50198956142280
  • UPC 10197106417577
  • UPC 50197106417575
  • UPC 10198956332010
  • UPC 50198956332018

Check against the official notice below — it lists the full affected range.

Hazard

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.

Details from the source

Reason for recall: 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. Distribution: US Nationwide distribution. Quantity: 846 units Lot/code info: 1) PBCCGRSGD, UDI-DI: 10197106840085(each), 50197106840083(case), Lot Number: NGKU0957 ; 2) PB35GYBJC, UDI-DI: 10197106375723(each), 50197106375721(case), Lot Number: NGKU2052 ; 3) PGVMOTBB19, UDI-DI: 10198956264113(each), 50198956264111(case), Lot Number: NGKT2394 ; 4) PGVM07C26, UDI-DI: 10198956264434(each), 50198956264432(case), Lot Number: NGKT2394 ; 5) PGVM07C27, UDI-DI: 10198956292895(each), 50198956292893(case), Lot Number: NGKT2394 ; 6) PGV2LTNHN, UDI-DI: 10198956292499(each), 50198956292497(case), Lot Number: NGKV2390 ; 7) PGV2LTNHN, UDI-DI: 10198956292499(each), 50198956292497(case), Lot Number: NGKV3390 ; 8) PG15OT92A, UDI-DI: 10197106475041(each), 50197106475049(case), Lot Number: NGKW2883 ; 9) PG23MLNLD, UDI-DI: 10198956432024(each), 50198956432022(case), Lot Number: NGKU3969 ; 10) PG29GCPCK, UDI-DI: 10198956299207(each), 50198956299205(case), Lot Number: NGKU4716 ; 11) PG29GCPC3, UDI-DI: 10198956532496(each), 50198956532494(case), Lot Number: NGKU4716 ; 12) PG33LVMNC, UDI-DI: 10198956188358(each), 50198956188356(case), Lot Number: NGKU1994 ; 13) PG33LVMNC, UDI-DI: 10198956188358(each), 50198956188356(case), Lot Number: NGKU1994 ; 14) PG33LVMNC, UDI-DI: 10198956188358(each), 50198956188356(case), Lot Number: NGKU1994 ; 15) PG33LVMNC, UDI-DI: 10198956188358(each), 50198956188356(case), Lot Number: NGKU1994 ; 16) PG35HPBJK, UDI-DI: 10198956124110(each), 50198956124118(case), Lot Number: NGKU0856 ; 17) PG35HPBJK, UDI-DI: 10198956124110(each), 50198956124118(case), L

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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