Steris Corporation: Accessories, Cleaning, For Endoscope
Recall Summary Steris Corporation is recalling RAPICIDE PA Part A High-Level Disinfectant (Model ML020115) because the vented cap can become blocked, causing gas to build up inside the bottle and potentially making it swell. When the cap is opened, this pressure may release excess vapor or liquid that could expose users to the disinfectant chemical if they are not wearing proper protective equipment. The 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
- FDA-DEVICES
- Recall date
- 2026-09-21
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Worldwide - US Nationwide distribution.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/c8194b24-ec73-4e01-bd7e-133eeeea8132