Smith & Nephew, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1239-2017)

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:

Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701

Product Classification:

Class II

Date Initiated: February 2, 2017

Date Posted: March 1, 2017

Recall Number: Z-1239-2017

Event ID: 76414

Reason for Recall:

The single use devices are provided sterile and do not have an expiration date on the label.

Status: Terminated

Product Quantity: 2646

Code Information:

Batch Numbers: 50586138 50458123 50418120 50339534 50306882 50285907 50248565 50231427 50197615 50171397 50158655 50138049 50119457 50089297 50082581 50069485

Distribution Pattern:

Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela

Voluntary or Mandated:

Voluntary: Firm initiated