ProductGuru Recalls

Official recall record

Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ROBOTIC PACK - 242561 Model No. MHRB88

US FDA — Medical Devices · 2026-08-10 · United StatesClass II
Issuing authority
US FDA — Medical Devices
Recall initiated by firm
2026-08-10
Country of alert
United States
Alert level
Class II
Alert type
recall
Barcode (EAN/GTIN)
0191072236531
Brand on record
American Contract Systems Inc
Product category
Medical Device

What the authority reported

Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the manufacturing process. Use of a contaminated wipe may lead to localized skin effects such as irritation, erythema, or mild inflammation. Failure to perform pericare due to disposal of contaminated wipes may increase risk of localized infection or catheter-associated urinary tract infection (CAUTI).

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-10-23.

More recalls: US FDA — Medical Devices · United States · all filters

Other recalls from this brand

All 21 official recall notices naming American Contract Systems Inc on this site →

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.