- Recalling firm
- Steris Corporation
- Reason for recall
- 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 products (lot / model / serial)
- 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 7/1/2027
- Units affected
- 11806 units
- Distribution pattern
- Worldwide - US Nationwide distribution.
- Firm location
- Mentor, OH, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-0155-2027
- Recall initiated
- September 21, 2026
- FDA classification date
- October 14, 2026
- FDA report date
- October 21, 2026
- FDA event ID
- 99804
- Last updated on HTM Vibe
- October 27, 2026
