There was a case that the swivel arm went down unintentionally when it was moved up/down.
There was a case that the swivel arm went down unintentionally when it was moved up/down.
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 Fujifilm Medical Systems U.S.A., Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-0385-2018 — Fujifilm Medical Systems U.S.A., Inc. Fujifilm Medical Systems U.S.A., Inc. recalls Aspire HD Plus Hello, I own a Fujifilm Medical Systems U.S.A., Inc. recalls Aspire HD Plus (FDR MS-2500), also known as Aspire HD Plus F and Aspire HD-s (FDR MS-2000), also known as Aspire HD that is covered by recall Z-0385-2018 from Fujifilm Medical Systems U.S.A., 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.
