Medline recalls blood pressure units with model numbers MDS4001, MDS4001LA, and MDS4001PLUS due to non-compliant manufacturing. Units may have been accepted into inventory without meeting specifications.
The firm provided a set of specifications for the device, but some units of the device were manufactured non-compliant with the specifications. However, the firms Receiving Dept. accepted these units into inventory
Medline is recalling blood pressure units with model numbers MDS4001, MDS4001LA, and MDS4001PLUS because some units were manufactured without meeting the required specifications. This could mean the units do not function as intended, but the recall does not specify a risk of injury or harm.
The units were manufactured without meeting the required specifications. This could lead to the device not functioning as intended, but the recall does not specify any risk of injury or harm.
Owners of blood pressure units with model numbers MDS4001, MDS4001LA, or MDS4001PLUS are affected. People using these units for home monitoring are most at risk if the device does not function correctly.
Check for model numbers MDS4001, MDS4001LA, or MDS4001PLUS on the device. Also look for specific lot numbers listed in the recall notice.
Identify the model number on your blood pressure unit to see if it matches MDS4001, MDS4001LA, or MDS4001PLUS.
The recall states that some units were manufactured non-compliant with specifications, but it does not mention any risk of injury or harm.
Check for model numbers MDS4001, MDS4001LA, or MDS4001PLUS on your device. Also look for the specific lot numbers listed in the recall notice.
The recall does not specify a remedy, so you may want to contact Medline directly for further guidance.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1459-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1459-2024 from Medline Industries. 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.
