Product Safety Recalls

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Aesculap Implant Systems LLC Recall 90537

Description: RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.

Aesculap Implant Systems LLC Recall 90537 Information

StatusCompleted
Mandated?Voluntary: Firm initiated
Recall NumberZ-1405-2022
Event ID90537
Event DescriptionRIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.
Product TypeDevices
DistributionUnited States: CO
Quantity2 pieces
Recall ReasonCustomized coronal rod benders may deform the implant when used with the spinal system devices.
Device Classification20220727
Device Code InfoLOT: 2930902A
Center Classification Date20220719
Recall Initiation Date20210630
Recalling FirmAesculap Implant Systems LLC
Initial Notification E-Mail
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