Steris Corporation recalls RAPICIDE PA Part A High-Level Disinfectant
- Recalling company
- Steris Corporation
- Product
- RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020115
- Reason
- If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid chemistry may escape from the bottle when the cap is twisted during opening, which could result in user exposure if required personal protective equipment (PPE) is not properly used. Such exposure may result in injury to the user or others in close proximity.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Sep 21, 2026
- Reported
- Oct 21, 2026
- Distribution
- Worldwide - US Nationwide distribution.
- Status
- Ongoing
- Quantity
- 374 units
- Lot / codes
- UDI: 00724995245658 Lot numbers with expiration dates: 687046 10/5/2027 688017 10/19/2027
- Company location
- Mentor, OH
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0154-2027
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0154-2027 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.