INSPIREMD recalls

6 recent recalls on record for INSPIREMD in connected official government data as of October 22, 2026 at 6:00 PM UTC.

Models with recalls

FDA Class II · Medical device · June 17, 2026

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Official ID Z-2330-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Official ID Z-2329-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Official ID Z-2328-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Official ID Z-2327-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Official ID Z-2326-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

Official ID Z-2325-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.