Spes Medica recalls
Spes Medica appears in 5 official U.S. recall notices indexed by RecallRadar, most recently on 2021-07-07.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Dragonfly Laryngeal Surface Electrode, ET Tube Size (mm): 7.5-10.0, Channel 1, Reference Numbers LSE4246MCA075 and LSE500M. for continuous…
FDA Device · Class II · 2021-07-07 · Spes Medica - Tripolar Hooked Stimulation Probes, L=20mm, Reference Number SI3H0020S2526D. Used during intraoperative neurological monitoring
FDA Device · Class II · 2021-07-07 · Spes Medica - Dragonfly Laryngeal Surface Electrode, ET Tube Size (mm): 6.0-7.5, Channel 2, Reference Number LSE3463DCA200 and LSE500DCS-5. for continuou…
FDA Device · Class II · 2021-07-07 · Spes Medica - SNS Disposable Urethral Catheter Electrode, 14 Fr, Gold Recording/Stimulating Contact printed on polyurethane film adhesive with attached 2…
FDA Device · Class II · 2021-07-07 · Spes Medica - SNS Disposable Urethral Catheter Electrode, 10 Fr, Gold Recording/Stimulating Contact printed on polyurethane film adhesive with attached 2…
FDA Device · Class II · 2021-07-07 · Spes Medica