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Recall Observatory FDA recall evidence

Device product

SwishPlus Implant 5.7mmD x 8mmL, SBM 6.5mmD Platform, Part Number 925708

Z-1126-2020

January 09, 2019

Class II

Product summary

Firm
Implant Direct Sybron Manufacturing LLC
Event
Event 84706
Status
Terminated
Classification
Class II
Quantity
11 units
Official record key
device-enforcement:Z-1126-2020

Official wording

Reason: Due to a complaint received and internal investigation it was determined that implant vials were distributed with incorrect color coded vials and caps. The part/lot numbers were correct, the customer received the product they ordered, however the color on the vial label and cap labels were incorrect.Specifically, the color coded vial and cap does not match the implant size described on the vial. As a result of the incorrect color on the vial and cap, the surgeon may not be certain if the implant received was the correct size. This could result in a delay in surgery, risk of infection if the surgical site has to be closed up and a second round of anesthesia.

Code information: Lot # 109038 No affected devices distributed within the US.

Distribution pattern: US: None OUS: Iceland, Sweden, Spain,

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    label and cap labels were incorrect