The Peristaltic Head tubing placed on the ARCHITECT c4000, c8000, and c16000 has the possibility to leak due to a manufacturing issue associated with the tubing connector.
The Peristaltic Head tubing placed on the ARCHITECT c4000, c8000, and c16000 has the possibility to leak due to a manufacturing issue associated with the tubing connector.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Abbott Laboratories, Inc to request your refund or repair — edit it as you like.
Subject: Recall Z-0166-2018 — Abbott Laboratories, Inc Abbott Laboratories, Inc recalls Tubing, Peristaltic Head Part Number 7-35 Hello, I own a Abbott Laboratories, Inc recalls Tubing, Peristaltic Head Part Number 7-35009685-01 for use in clinical chemistry systems. that is covered by recall Z-0166-2018 from Abbott Laboratories, Inc. 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.
