Official recall record
RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020117
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2026-09-21
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00724995245962
- Brand on record
- Steris Corporation
What the authority reported
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
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.
Record last checked against the registry on 2026-11-12.
Other recalls from this brand
- 2026-09-23 · US FDA — Medical Devices
HexaVue Focus Integration System, a single, all-in-one system that handles operating room video routing, surgi - 2026-09-21 · US FDA — Medical Devices
RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020115 - 2026-09-21 · US FDA — Medical Devices
RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020116
All 13 official recall notices naming Steris Corporation on this site →