Preat Corp recalls Astra EV-compatible 4.2mm digital analog devices with a 180-degree calibration error. Affected units may not function correctly due to manufacturing defect.
Due to manufacturing error, digital analog rotational feature is 180 degrees off.
Preat Corp is recalling Astra EV-compatible 4.2mm digital analog devices because a manufacturing error causes the rotational feature to be 180 degrees off. This could lead to incorrect readings or functionality issues.
The device's rotational feature is 180 degrees off due to a manufacturing error. This could cause incorrect readings or functionality issues, especially in applications requiring precise calibration.
Users of the Preat Astra EV-compatible 4.2mm digital analog devices with model numbers 9006603 (single) or 9006603-10 (10-pack) are affected. Most at risk are those using the device for precise measurements where calibration accuracy matters.
Check for model numbers 9006603 (single) or 9006603-10 (10-pack) on the device. The product is sold as Rx Only (prescription-only) and was manufactured in lots 278735, 278402, or with UDI codes.
Identify the model number on the device to confirm if it is 9006603 or 9006603-10.
Due to a manufacturing error, the digital analog rotational feature is 180 degrees off, which could cause incorrect readings or functionality issues.
The recall record does not specify a remedy, so no action is required beyond checking if your device matches the model numbers listed.
The device may not function correctly due to the calibration error, but it does not pose a risk of injury or damage under normal use.
We’ve drafted a message you can send Preat to request your refund or repair — edit it as you like.
Subject: Recall Z-2107-2025 — Preat Preat Hello, I own a Preat that is covered by recall Z-2107-2025 from Preat. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
