Quick summary: NephroMax High Pressure Nephrostomy Balloon Catheter. Reason: Health product recall. Category: Health products. Date: 2026-07-02.
NephroMax High Pressure Nephrostomy Balloon Catheter
2026-07-02
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: NephroMax High Pressure Nephrostomy Balloon Catheter. Reason: Health product recall. Category: Health products. Date: 2026-07-02.
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
Affected products
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.
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
Frequently asked questions
Answers based on the official recall notice.
Product images
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