Sakura Finetek USA Inc: Medical Device Recall in 2014 - (Recall #: Z-1748-2014)

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:

Tissue-Tek PARAFORM PROC/EMB/MEDIUM, FORMULA 3 - 8x1Kg. for diagnostic chemistry use. Sakura Finetek USA, Inc.

Product Classification:

Class II

Date Initiated: April 16, 2014

Date Posted: June 18, 2014

Recall Number: Z-1748-2014

Event ID: 68081

Reason for Recall:

This Lot has variations in melting temperature.

Status: Terminated

Product Quantity: 115

Code Information:

Product Code: 7052. Lot Number: 263922.

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated