Polymer Technology Systems recalls CHOL+HDL+GLU test strips REF 2412 due to potential incorrect results from test strips falling out during analysis. Affected lots include I808, I809, I811, I812, I814.
Some lots of test strips do not fit tightly into the optical block, and may fall out during analysis, which could lead to an incorrect result being displayed
Polymer Technology Systems is recalling CHOL+HDL+GL: test strips with reference number 2412 because some lots may fall out during analysis, leading to incorrect results. This could affect users who rely on these strips for accurate health monitoring.
The test strips may not fit tightly into the optical block and could fall out during analysis. This might cause the device to display an incorrect result, potentially leading to inaccurate health monitoring.
People who own or use the CHOL+HDL+GLU test strips with reference number 2412, particularly those who test blood glucose levels regularly. Those using the affected lots (I808, I809, I811, I812, I814) are most at risk.
Check the reference number on the test strips. Affected lots are I808, I809, I811, I812, and I814. The product is sold under reference number 2412.
Look for the reference number 2412 on the test strips to confirm if they are affected.
Some lots of test strips do not fit tightly into the optical block and may fall out during analysis, which could lead to incorrect results being displayed.
Affected lots include I808, I809, I811, I812, and I814.
The recall record does not specify a remedy, so no action is required beyond checking the reference number.
We’ve drafted a message you can send Polymer Technology Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-1373-2019 — Polymer Technology Systems Polymer Technology Systems Hello, I own a Polymer Technology Systems that is covered by recall Z-1373-2019 from Polymer Technology Systems. 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.
