Siemens Healthcare recalls Syva EMIT II Plus 6-Acetyl morphine 28mL catalog #9R039UL for incorrect calibrator level in calibration steps. No remedy specified in recall notice.
Incorrect calibrator level listed in qualitative calibration steps
Siemens Healthcare is recalling Syva EMIT II Plus 6-Acetyl morphine 28mL test kits (catalog #9R039UL) because the calibration steps list an incorrect calibrator level. This could lead to inaccurate test results if used without correction.
The calibration steps in the test kit list an incorrect calibrator level. This could cause inaccurate test results if the user follows the steps without correcting the level. Inaccurate results might lead to wrong medical decisions.
Users of the Syva EMIT II Plus 6-Acetyl morphine 28mL test kits (catalog #9R039UL) who perform medical testing. Those with medical conditions requiring precise testing may be at slightly higher risk.
Check for the Syva EMIT II Plus 6-Acetyl morphine 28mL test kits with catalog number 9R039UL. All lots are affected by this recall.
Identify if your test kit has catalog number 9R039UL for 28mL.
The recall notice does not specify a remedy.
Check for the Syva EMIT II Plus 6-Acetyl morphine 28mL test kit with catalog number 9R039UL.
The recall does not require immediate stop use; check if your kit is affected first.
We’ve drafted a message you can send Siemens Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1800-2018 — Siemens Healthcare Siemens Healthcare Hello, I own a Siemens Healthcare that is covered by recall Z-1800-2018 from Siemens Healthcare. 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.
