Ortho-Clinical recalls VITROS XT 7600 Integrated Systems that may cause delayed test results if MicroTip Pack caps aren't properly removed or replaced.
MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip Pack Caps on VITROS¿ 5600 and XT 7600 Integrated Systems, results may be delayed results if a pack becomes unusable
Ortho-Clinical is recalling VITROS XT 7600 Integrated Systems because the MicroTip Pack Opener Assembly might not remove or replace MicroTip Pack caps, leading to delayed test results if a pack becomes unusable.
The MicroTip Pack Opener Assembly might not properly remove or replace MicroTip Pack caps. This can cause the packs to become unusable, resulting in delayed test results.
Healthcare facilities using the VITROS XT 7600 Integrated System for clinical testing are most likely affected. Patients receiving tests using this system could experience delayed results if the MicroTip Pack caps aren't properly handled.
Check for the product code 6844461 and serial numbers J76000109 to J76001492 on the VITROS XT 7600 Integrated System. This system is used for clinical testing and was sold with specific model numbers.
Ensure the MicroTip Pack caps are properly removed and replaced to avoid delayed test results.
The MicroTip Pack Opener Assembly may not properly remove or replace MicroTip Pack caps, which can cause packs to become unusable and lead to delayed test results.
Check if your VITROS XT 7600 Integrated System has the product code 6844461 and serial numbers J76000109 to J76001492. If so, ensure MicroTip Pack caps are properly handled to avoid delayed results.
The recall does not specify a fix; users must ensure proper handling of MicroTip Pack caps to prevent delayed results.
We’ve drafted a message you can send Ortho-Clinical to request your refund or repair — edit it as you like.
Subject: Recall Z-1555-2023 — Ortho-Clinical Ortho-Clinical Hello, I own a Ortho-Clinical that is covered by recall Z-1555-2023 from Ortho-Clinical. 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.
