Urgent Field Safety Notice For (kit) Imp Tumorstent, (kit) Innoflex Mono-j, (kit) Innoflex Ureteral Stent, (kit) Innosoft Mono-j, (kit) Innosoft Ureteralstent, (kit) Innostar Ureteralstent, (kit) Perc
Recall Summary BS Medical Tech Industry is issuing an urgent safety notice for multiple ureteral stent and nephrostomy drainage kits used in urological procedures. The specific reason for the recall is not detailed in this notice. These products were distributed in Germany and the EU, and this is classified as a Class I recall, indicating a serious safety concern.
- Recalling firm
- BS Medical Tech Industry
- Product
- (Kit) IMP Tumorstent, (Kit) Innoflex Mono-J, (Kit) Innoflex Ureteral stent, (Kit) Innosoft Mono-J, (Kit) Innosoft Ureteralstent, (Kit) Innostar Ureteralstent, (Kit) Percudrain 2 step nephrostomy, (Kit) Percudrain 3, (Kit) Percusof
- Reason
- Urgent Field Safety Notice for (Kit) IMP Tumorstent, (Kit) Innoflex Mono-J, (Kit) Innoflex Ureteral stent, (Kit) Innosoft Mono-J, (Kit) Innosoft Ureteralstent, (Kit) Innostar Ureteralstent, (Kit) Percudrain 2 step nephrostomy, (Kit) Percudrain 3, (Kit) Percusof by BS Medical Tech Industry
- Classification
- Class I
- Category
- medical device recall
- Country
- Germany
- Agency
- BFARM
- Recall date
- 2026-11-02
- Status
- Ongoing
- Distribution
- Germany / EU
Official recall notice from BFARM
Recall details on Nibble Recalls: https://trynibble.app/recalls/084a9aab-c0c4-4e74-baf8-5fa7bfa780d0