PlainRecalls
FDA Devices Moderate Class II Terminated

Tripolar Hooked Stimulation Probes, L=20mm, Reference Number SI3H0020S2526D. Used during intraoperative neurological monitoring.

Reported: July 7, 2021 Initiated: April 8, 2021 #Z-1971-2021

Product Description

Tripolar Hooked Stimulation Probes, L=20mm, Reference Number SI3H0020S2526D. Used during intraoperative neurological monitoring.

Reason for Recall

The supplier informed them of possible deviations of the parameters/processes defined for ethylene oxide sterilization.

Details

Recalling Firm
Spes Medica
Units Affected
3 boxes
Distribution
Distribution in the following US states: CA, MA, and SC.
Location
Genoa, N/A

Frequently Asked Questions

What product was recalled?
Tripolar Hooked Stimulation Probes, L=20mm, Reference Number SI3H0020S2526D. Used during intraoperative neurological monitoring.. Recalled by Spes Medica. Units affected: 3 boxes.
Why was this product recalled?
The supplier informed them of possible deviations of the parameters/processes defined for ethylene oxide sterilization.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 7, 2021. Severity: Moderate. Recall number: Z-1971-2021.