Steris Corp C1141 Flexible Endoscope Processing Container, designed to fit the Steris System I Processor. The unit may be sold individually or with the processing tray assembly (C1140). Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
C1141 Flexible Endoscope Processing Container, designed to fit the Steris System I Processor. The unit may be sold individually or with the processing tray assembly (C1140).
Brand
Steris Corp
Lot Codes / Batch Numbers
All codes.
Products Sold
All codes.
Steris Corp is recalling C1141 Flexible Endoscope Processing Container, designed to fit the Steris System I Processor. The due to The container flow port is inverted, which restricts the flow of sterilant to the endoscope and affects the sterilization process.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The container flow port is inverted, which restricts the flow of sterilant to the endoscope and affects the sterilization process.
Recommended Action
Per FDA guidance
The firm notified their customers by telephone and letter on 4/23/2003.
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 noticePage updated: Jan 10, 2026