Midmark Corp Midmark M7 UltraClave and Ritter M7 SpeedClave, Tabletop Steam Sterilizers. Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Midmark M7 UltraClave and Ritter M7 SpeedClave, Tabletop Steam Sterilizers.
Brand
Midmark Corp
Lot Codes / Batch Numbers
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.
Products Sold
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.
Midmark Corp is recalling Midmark M7 UltraClave and Ritter M7 SpeedClave, Tabletop Steam Sterilizers. due to The pressure relief valve may fail to open properly.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The pressure relief valve may fail to open properly.
Recommended Action
Per FDA guidance
The firm notified their customers by telephone on 3/5/2003.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, CA, FL, IL, IN, ME, MA, MO, NH, OH, VA
Page updated: Jan 10, 2026