Medtronic: Medical Device Recall in 2017 - (Recall #: Z-2545-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: May 3, 2017

Date Posted: June 21, 2017

Recall Number: Z-2545-2017

Event ID: 77144

Reason for Recall:

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

Status: Terminated

Product Quantity: 478,465 (total for all products)

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.

Voluntary or Mandated:

Voluntary: Firm initiated