Steris Corporation: Rapicide Pa Part A High-level Disinfectant, Model/catalog Number: Ml020115
Summary Steris Corporation is recalling RAPICIDE PA Part A High-Level Disinfectant (Model ML020115) because a blocked vent cap can cause gas buildup and pressure inside the bottle, potentially leading to swelling or leaking of vapor or liquid when opened. Users who don't wear proper protective equipment could be exposed to the disinfectant, risking injury to themselves or others nearby. This product has been distributed nationwide across the United States.
- Recalling firm
- 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
- Category
- medical device recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-09-21
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Worldwide - US Nationwide distribution.
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/2202e63a-5fb5-4dec-b926-eac6a77bc7a9