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Recall Observatory FDA recall evidence

Device product

AESCULAP S4 Cervical Cross Connector L22mm, S4C CROSS CONNECTOR FIXED 22MM, product code SW112T. Used in spinal fusion surgery.

Z-1443-2022

September 08, 2020

Class II

Product summary

Firm
Aesculap Implant Systems LLC
Event
Event 90502
Status
Terminated
Classification
Class II
Quantity
24
Official record key
device-enforcement:Z-1443-2022

Official wording

Reason: Insufficient clamping force of the cross connectors in the spinal surgical system which may lead to movement of the connectors on the rods and/or microparticle abrasion.

Code information: UDI-DI: 04038653362295

Distribution pattern: United States Nationwide distribution in the states of CA, CO, IL, IN, MI, NC, NV, OH, PA, SC, TX & WY.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Insufficient clamping force of the cross connectors in the spinal surgical system which may lead to movement of the connectors on the rods and/or microparticle abrasion.