Medela recalls Invia Motion Negative Pressure Wound Therapy systems with battery missing error display. Affected models include Endure (087.4010) and 15/60-day therapy versions. No remedy specified in recall notice.
Device may display a battery missing error.
Medela is recalling certain Invia Motion Negative Pressure Wound Therapy systems that may display a battery missing error. This could potentially affect device operation but does not involve immediate safety risks like injury or fire. The recall does not include a specific remedy.
The device may show a battery missing error message, which could indicate a temporary issue with the battery system. This might cause the device to malfunction temporarily but does not pose a risk of injury or serious harm during normal use.
Patients using Medela's Invia Motion Negative Pressure Wound Therapy systems with specific model numbers (087.4010, 087.4012, etc.) for wound care. Those with the listed serial numbers are most at risk.
Check for model numbers: Endure (087.4010), 15-day (087.4012), 60-day (087.4014), or Endure (087.4020) versions. Also look for the listed serial numbers in the product details.
Look for a battery missing error message on the device display. If present, the device may need to be reset or checked for battery issues.
The recall notice does not specify a remedy for the battery missing error. Users should check the device status and contact Medela for assistance if needed.
Affected models include Endure Negative Pressure Wound Therapy (087.4010), 15 Days Negative Pressure Wound Therapy (087.4012), 60 Days Negative Pressure Wound Therapy (087.4014), and similar variants with specific serial numbers listed in the recall.
No, the recall does not require stopping use. The device may display a temporary battery error but does not pose a risk of injury or serious harm.
We’ve drafted a message you can send Medela to request your refund or repair — edit it as you like.
Subject: Recall Z-2528-2018 — Medela Medela Hello, I own a Medela that is covered by recall Z-2528-2018 from Medela. 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.
