- 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: 00724995245658 Lot numbers with expiration dates: 687046 10/5/2027 688017 10/19/2027
- Units affected
- 374 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-0154-2027
- 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
