There is a potential for the over-pressure safety (OPS) valve in the tubing kits to not allow flow through.
There is a potential for the over-pressure safety (OPS) valve in the tubing kits to not allow flow through.
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 Datascope Corporation to request your refund or repair — edit it as you like.
Subject: Recall Z-2180-2018 — Datascope Corporation Datascope Corporation recalls Maquet Cardiopulmonary Bypass Custom Tubing kit Hello, I own a Datascope Corporation recalls Maquet Cardiopulmonary Bypass Custom Tubing kit BO-TOP 38600 ADULT CPB, Part Number 701056035R01 Product Usage: The that is covered by recall Z-2180-2018 from Datascope Corporation. 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.
