FDA recall record

Preat recall — FDA Z-2107-2025

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

Class IIclassification
Z-2107-2025official record ID
Jul 16, 2025report date

Recall record at a glance

Official recordZ-2107-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmPreat Corp
Report dateJul 16, 2025
Recall initiation dateJun 24, 2025
Quantity44 units
LocationSanta Maria, CA, United States

Official product description

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

Why the product was recalled

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

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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