FDA-Device2026-10-21Class IIPACKAGING DEFECT

Steris RAPICIDE PA Part A disinfectant recalled for pressurized bottle hazard

Nationwide distributionMedical devices

What this means

The vented cap on this high-level disinfectant bottle can become blocked, causing gas to build up inside. When the pressure increases, the bottle may swell, and opening it could release vapor or liquid that may expose users to the chemical if protective equipment is not properly worn.

  • Check if you have RAPICIDE PA Part A (Model ML020115) with lot numbers 687046 or 688017.
  • Do not open or use affected bottles.
  • Contact Steris Corporation for instructions on how to return or dispose of your product safely.
  • Wear appropriate PPE if you must handle the bottle before returning it.
Get recalls like this in a free plain-English brief every Sunday.Get alerts ↓
The agency's original wording
Hazard

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.

Intended for
All ages
Illnesses reported
None reported
Sold states
Worldwide - US Nationwide distribution.
Affected count
374 units
Manufactured in
5960 Heisley Rd, Mentor, OH, United States
Products
RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020115

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0154-2027

More Steris recalls

Want us to check the next one for you?

We read every CPSC, FDA, USDA, and NHTSA notice and email you a plain-English Sunday brief covering your household — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.

Free · One email a week · Unsubscribe anytime
By signing up you agree to our Terms and Privacy Policy.