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Recall Observatory FDA recall evidence

Device product

Best Practice Kit, Item Numbers: 00Z2064, 00Z2150, 00Z2190, 00Z2192, 00Z2211, 00Z2212, 00Z2216, 00Z2217, 00Z2312

Z-2545-2017

May 03, 2017

Class II

Product summary

Firm
Medtronic
Event
Event 77144
Status
Terminated
Classification
Class II
Quantity
478,465 (total for all products)
Official record key
device-enforcement:Z-2545-2017

Official wording

Reason: Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.

Code information: N/A

Distribution pattern: Worldwide distribution. US Nationwide including PR, and countries of AU, BE, CA, CL, CN, IL, IT, JP, KR, MX, PA, SA, SG, and TR.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    incomplete seal