Nephrostomy Catheter
Nephrostomy Catheter Recall Summary Boston Scientific is recalling certain NephroMax™ High Pressure Nephrostomy Balloon Catheters and related urology procedure kits because the renal sheath may be packaged in the wrong orientation. This recall applies to products distributed to hospitals, pharmacies, and laboratories in New Zealand. This is classified as a Class I recall, the most serious type.
- Recalling firm
- Boston Scientific NZ Ltd
- Product
- Nephrostomy Catheter. [Device]. Also covers: Urology Procedure Kits
- Reason
- The manufacturer had been made aware that the renal sheath for certain NephroMax™ High Pressure Nephrostomy Balloon Catheters may be packaged in a reversed orientation.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-06-22
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/114d981a-1f9b-4955-ad9b-e4a94f46f1aa