Health product recall

NephroMax High Pressure Nephrostomy Balloon Catheter

Last updated

Summary

Product
NephroMax High Pressure Nephrostomy Balloon Catheter
Issue
Medical devices - Device compatibility
What to do

Contact the manufacturer if you require additional information.

Affected products

Affected products Lot or serial number Model or catalogue number
NephroMax High Pressure Nephrostomy Balloon Catheter More than 10 numbers, contact manufacturer. M0062101180
NephroMax High Pressure Nephrostomy Balloon Catheter More than 10 numbers, contact manufacturer. M0062101420
NephroMax High Pressure Nephrostomy Balloon Catheter More than 10 numbers, contact manufacturer. M0062101620
NephroMax High Pressure Nephrostomy Balloon Catheter More than 10 numbers, contact manufacturer. M0062101440
NephroMax High Pressure Nephrostomy Balloon Catheter More than 10 numbers, contact manufacturer. M0062101170
NephroMax High Pressure Nephrostomy Balloon Catheter More than 10 numbers, contact manufacturer. M0062101400
NephroMax High Pressure Nephrostomy Balloon Catheter More than 10 numbers, contact manufacturer. M0062101600
NephroMax High Pressure Nephrostomy Balloon Catheter More than 10 numbers, contact manufacturer. M0062101640

Issue

Boston Scientific is notifying you that the renal sheath for certain NephroMax™ high pressure nephrostomy balloon catheters may be packaged in a reversed orientation.

Between November 2025 and April 2026, seven (7) complaints reported reversed sheath orientation upon opening. In all cases, the issue was identified and corrected prior to patient use. If the sheath orientation is not corrected prior to use, the non-tapered end may be inserted in the patient, which could increase resistance and result in difficulty advancing, withdrawing or positioning the catheter. The potential for patient harm is considered low because the issue is readily identifiable and can be corrected prior to use.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Gastroenterology and urology
Companies
Boston Scientific Corporation
300 Boston Scientific Way, Marlborough, Massachusetts, United States, 01752
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Recall date
Identification number
RA-82276

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