Preat Corp: Medical Device Recall in 2025 - (Recall #: Z-2107-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx Only

Product Classification:

Class II

Date Initiated: June 24, 2025

Date Posted: July 16, 2025

Recall Number: Z-2107-2025

Event ID: 97136

Reason for Recall:

Due to manufacturing error, digital analog rotational feature is 180 degrees off.

Status: Ongoing

Product Quantity: 44 units

Code Information:

Lots: 278735, & 278402/UDI:

Distribution Pattern:

US Nationwide distribution in the states of AL, CA, FL, GA, KY, MD, MN, NY, OK, PA.

Voluntary or Mandated:

Voluntary: Firm initiated