Blue Belt Technologies MN: Medical Device Recall in 2014 - (Recall #: Z-1942-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Stride Femoral Component Size 2, PFSI-00053, Right Lateral /Left Medial. Unicondylar Knee prosthesis.

Product Classification:

Class II

Date Initiated: June 4, 2014

Date Posted: July 9, 2014

Recall Number: Z-1942-2014

Event ID: 68482

Reason for Recall:

Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains PFSI-00054, Right Medial/Left lateral implants. Packages labeled PFSI-00054, Stride Right Medial/Left Lateral contain PFSI-00053, Left Medial/Right Lateral.

Status: Terminated

Product Quantity: 2

Code Information:

Lot C785231, Exp 5-2015

Distribution Pattern:

US Nationwide Distribution in the states of CA, PA, and TX

Voluntary or Mandated:

Voluntary: Firm initiated