OVERLOOKED

Recalls › Medicines & devices

Class IIOngoing

Steris Corporation recalls 3 products

Recall date · record updated Oct 21, 2026 · Source: U.S. Food and Drug Administration (openFDA device enforcement)

What to do

Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.

Company
Steris Corporation
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.
Hazard
FDA Class II: may cause temporary or medically reversible adverse health consequences (FDA definition).
Who’s affected
Worldwide - US Nationwide distribution.
Where
Nationwide
Official notice
www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99804…

Products (3)

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

    Codes/lots: UDI: 00724995245658 Lot numbers with expiration dates: 687046 10/5/2027 688017 10/19/2027Quantity: 374 unitsRecall no. Z-0154-2027Class II

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

    Codes/lots: UDI: 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 7/1/2027Quantity: 11806 unitsRecall no. Z-0155-2027Class II

  3. RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020117

    Codes/lots: UDI: 00724995245962 Lot numbers with expiration dates: 688019 10/19/2027 688021 10/19/2027 688023 10/19/2027 688025 10/19/2027 688576 10/26/2027 688580 10/26/2027 688582 10/26/2027 688584 10/26/2027 688586 10/26/2027 688588 10/26/2027 689173 11/2/2027 689175 11/2/2027 689177 11/2/2027 689179 11/2/2027 689983 11/10/2027 689985 11/10/2027 689987 11/10/2027 690299 11/16/2027 690301 11/16/2027 690995 11/24/2027 690997 11/24/2027 690999 11/24/2027 691001 11/24/2027 691741 12/1/2027 691743 12/1/2027 691745 12/8/2027 692203 12/8/2027 692206 12/8/2027 692208 12/8/2027 692210 12/8/2027 692213 12/8/2027Quantity: 106758 unitsRecall no. Z-0156-2027Class II

Update history

  1. First listed on OVERLOOKED from the official record.

When the agency expands or changes this recall, we update this page and log the change here.

Proof: raw official record (JSON) · fetched from FDA API

More Medicines & devices recalls