FDA Medical Device Recalls (openFDA)
Midmark Corp: Midmark M7 UltraClave and Ritter M7 SpeedClave, Tabletop Steam Sterilizers.
- Recall number
- Z-0704-03
- Recalling firm
- Midmark Corp
- Product
- Midmark M7 UltraClave and Ritter M7 SpeedClave, Tabletop Steam Sterilizers.
- Status
- Terminated
- Initiated
- 2003-03-05
- Posted
- 2003-04-01
- Terminated
- 2004-01-20
- Reason
- The pressure relief valve may fail to open properly.
- Root cause
- Other
- Action
- The firm notified their customers by telephone on 3/5/2003.
- Quantity
- 35
- Distribution
- The units were shipped to distributors and medical facilities located in: ME, IL, CA, VA, MA, MO, AZ, OH, IN, NH, and FL. The units were also distributed into Canada.
- Lot, serial or model codes
- Models: M7-011 and M7-014; Serial Numbers: MH006260 to MH006269, MH006273, MH006277 to MH006282, MH006284 to MH006290, MH006294, ML007606 to ML007608, ML007610, ML007637 to ML007642.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FLE
- Firm FEI
- 1523530
- Firm city
- Versailles
- Firm state
- OH
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28