Reported Oct 21, 2026 · Ongoing · Updated Oct 26, 2026

RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020115

Steris Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Steris Corporation · 5960 Heisley Rd · Mentor, OH · 44060-1834

Is this the product you have?

  • RAPICIDE PA Part A High-Level Disinfectant
  • Model/Catalog NumberML020115
Lot codes and dates
  • UDI00724995245658
  • Lot numbers with expiration dates687046 10/5/2027 688017 10/19/2027
Amount recalled
374 units

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Nov 4, 1:18 AM UTC

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