No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
No image published for this recall
Nephromax high pressure nephrostomy balloon catheter
Official notice
2 Jul 2026
An official Health Canada notice concerns Nephromax high pressure nephrostomy balloon catheter. 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. Published 2026-07-02.
What to do now
Contact the manufacturer if you require additional information.
Recall number
82276
Official notice
2026-07-02
The hazard
The hazard
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.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Skus
Other
Model Numbers
Recall Numbers
Checked manually this time?
The app alerts you when a new official recall is published — no searching, no checking back.
Turn on recall alertsAffected products
Affected products
Product 1
Product 2
Product 3
Product 4
Product 5
Product 6
Product 7
Product 8
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Boston Scientific.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
View full official noticeRelated recalls
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Cre™ wireguided and cre pro™ wireguided balloon dilation catheters
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Hot axios™ stent and electrocautery-enhanced delivery system
Brand match
High risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Iceseed 1.5 cx 90 needle
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Ams 700™ inflatable penile prosthesis with tenacio™ pump
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Hot axios™ stent and electrocautery enhanced delivery system
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Wallflex™ esophageal fully covered partially covered stent systems
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Capio™ slim suture capturing device
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Autotome rx
Brand match
Critical risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Exalt model d single-use duodenoscope
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Habib™ endohpb catheter
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Exalt model d single-use duodenoscope
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Solar™ gi
Brand match
Critical risk
Markets
Weekly recall digest
Get next week's recalls before you need them.
One email every Monday — official-source recalls for your country, and nothing else. Unsubscribe from any email.
The digest is the slow lane — one email a week. For instant, severity-gated alerts the moment a notice is published, get the app.
This recall was published 2 Jul 2026. The next one won't wait for you to search.
RecallScope watches official sources for the brands and VINs you follow, and alerts you the moment a new notice is published.