Urgent Field Safety Notice For Innova Igs 5 & 6 - Allia Igs 3, 5 & 5 Pulse By Ge Medical Systems Scs
I'm unable to provide an accurate summary because the recall document you've provided doesn't contain clear information about what the safety issue actually is. The text appears to be corrupted or incomplete, with repeated header information but no explanation of the specific hazard or risk. To summarize this recall properly, I would need the actual reason/hazard section of the notice. Could you provide the complete document or the specific safety concern?
- Recalling firm
- Urgent Field Safety Notice for Innova IGS 5 & 6 - Allia IGS 3, 5 & 5 Pulse by GE Medical Systems SCS , Download_Veroeffe
- Product
- s Tasks of the BfArM Risk assessment Field corrective actions Urgent Field Safety Notice for Innova IGS 5 & 6 - Allia IGS 3, 5 & 5 Pulse by GE Medical Systems SCS 2026
- Reason
- assessment Field corrective actions Urgent Field Safety Notice for Innova IGS 5 & 6 - Allia IGS 3, 5 & 5 Pulse by GE Medical Systems SCS 2026
- Classification
- Class I
- Category
- medical device recall
- Country
- Germany
- Agency
- BFARM
- Recall date
- 2026-06-17
- Status
- Ongoing
- Distribution
- Germany / EU
Official recall notice from BFARM
Recall details on Nibble Recalls: https://trynibble.app/recalls/e9ce10d9-1230-47c8-90f8-9b8103bab4b3