LABORIE MEDICAL TECHNOLOGIES, CANADA ULC Pump Tube Set for MMS Libra and Solar Systems - Product Usage: Intended for use during water perfusion urodynamic procedures to study the function of the bladder and urethra during filling and voiding, by monitoring pressure and pressure changes. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Pump Tube Set for MMS Libra and Solar Systems - Product Usage: Intended for use during water perfusion urodynamic procedures to study the function of the bladder and urethra during filling and voiding, by monitoring pressure and pressure changes.
Brand
LABORIE MEDICAL TECHNOLOGIES, CANADA ULC
Lot Codes / Batch Numbers
Model Number: REF 902101226, LOT 15883/1
Products Sold
Model Number: REF 902101226, LOT 15883/1
LABORIE MEDICAL TECHNOLOGIES, CANADA ULC is recalling Pump Tube Set for MMS Libra and Solar Systems - Product Usage: Intended for use during water perfusi due to This field correction is being initiated to address potentially damaged seals in the packaging of some the Laborie Pump Tube Sets. Finished goods inve. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
This field correction is being initiated to address potentially damaged seals in the packaging of some the Laborie Pump Tube Sets. Finished goods inventory was detected with damage to their seals in the form of breaches or folds. Based on our investigation the issue appears to be limited to a single lot of part number 902101226 pump tubing sets.
Recommended Action
Per FDA guidance
This field correction is being initiated to address potentially damaged seals in the packaging of some the Laborie Pump Tube Sets. Finished goods inventory was detected with damage to their seals in the form of breaches or folds. Based on our investigation the issue appears to be limited to a single lot of part number 902101226 pump tubing sets.
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