RecallRadar

FDA Device recall Z-0155-2027

RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020116

On 2026-10-21 the FDA classified a Class II recall of RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020116 by Steris, citing 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….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0155-2027
ClassificationClass II
Statusongoing
Initiated2026-09-21
Published2026-10-21
Last updated2026-10-27 05:30 UTC
CompanySteris
DistributionUS

Product

RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020116

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.

Identifiers

code_infoUDI: 00724995245955 Lot numbers with expiration dates: 689171 5/4/2027 689981 5/12/2027 690993 5/26/2027 691739 6/2/2027 692570 6/11/2027 694357 7/1/2027

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-10-27 05:30 UTC. Current status: ongoing.

Other recalls by Steris

All Steris recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0155-2027%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.