FDAFDA recall Z-0154-2027 · Oct 21, 2026
Steris Corporation: RAPICIDE PA Part A High-Level Disinfectant recall
Recall found
Product
RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020115
Reason for recall
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.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- UDI: 00724995245658 Lot numbers with expiration dates: 687046 10/5/2027 688017 10/19/2027
- Quantity
- 374 units
- Distribution
- Worldwide - US Nationwide distribution.
- Recalling firm
- Steris Corporation, Mentor, OH
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-09-21
Source: openFDA enforcement record Z-0154-2027 · search recall number Z-0154-2027 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 26, 2026, 8:14 PM EDT. The agency notice is the final word.