FDA Medical Device · Z-0154-2027

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

Class II · Ongoing

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.

Affected lots / codes — check yours against thisUDI: 00724995245658 Lot numbers with expiration dates: 687046 10/5/2027 688017 10/19/2027

Recalling firm: Steris Corporation, Mentor, OH
Classification: Class II (temporary or reversible harm possible)
Status: Ongoing
Quantity: 374 units
Distribution: Worldwide - US Nationwide distribution.
Recall initiated: September 21, 2026
Classified: October 14, 2026
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0154-2027%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

Check this brand across all 8 databases →