R A Medical Services recalls MINISCAV vacuum pumps with serial numbers N/AB/10514 to N/AB/1:23 due to inadequate documentation of acceptance activity. No remedy specified in recall notice.
Inadequate documentation of acceptance activity
R A Medical Services is recalling MINISCAV vacuum pumps with specific serial numbers because the documentation for acceptance activity was inadequate. This could lead to improper use or safety issues if the documentation is missing.
The hazard involves inadequate documentation of acceptance activity, which means the pump's proper use and safety might not be verified. This could lead to improper operation or safety risks if the documentation is missing or incorrect.
Medical professionals using MINISCAV vacuum pumps with serial numbers N/AB/10514 through N/AB/10523 are most at risk. The recall affects devices that were sold with incomplete acceptance documentation.
Check the serial number on the MINISCAV vacuum pump, which ranges from N/AB/10514 to N/AB/10523. The product was sold with inadequate documentation of acceptance activity.
Identify the serial number on the MINISCAV vacuum pump to confirm if it falls within the range N/AB/10514 to N/AB/10523.
The recall notice does not specify any remedy.
Check the serial number to see if it is within the range N/AB/10514 to N/AB/10523. If it is, contact R A Medical Services for further instructions.
Look for the serial number on the pump, which should be between N/AB/10514 and N/AB/10523. The product was sold with inadequate documentation of acceptance activity.
We’ve drafted a message you can send R A Medical Services to request your refund or repair — edit it as you like.
Subject: Recall Z-2619-2023 — R A Medical Services R A Medical Services Hello, I own a R A Medical Services that is covered by recall Z-2619-2023 from R A Medical Services. 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.
