CLASS II Device recall · Reported 1 Aug 2018 · FDA Enforcement Report
Invia Motion Negative Pressure Wound Therapy System recalled by Medela
Medela is recalling Invia Motion Negative Pressure Wound Therapy System, distributed nationwide in the US. The recall was initiated on 7 Feb 2018 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2528-2018
- FDA event ID
- 80078
- Recalling firm
- Medela, McHenry, IL
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 7 Feb 2018
- FDA classified
- 23 Jul 2018
- Reported
- 1 Aug 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Device Malfunction
- Device type
- Other Medical Devices
Timeline
| 7 Feb 2018 | Recall initiated by company | |
| 23 Jul 2018 | Classified by FDA | +166 days |
| 1 Aug 2018 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Device may display a battery missing error.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Endure Negative Pressure Wound Therapy (Model 087.4010); b. 15 Days Negative Pressure Wound Therapy (Model 087.4012); c. 60 Days Negative Pressure Wound Therapy (Model 087.4014); d. Endure Negative Pressure Wound Therapy (Model 087.4020 ); e. 15 Days Negative Pressure Wound Therapy (Model 087.4022); f. 60 Days Negative Pressure Wound Therapy (Model 087.4024). Product Usage: The Invia Motion Negative Pressure Wound Therapy (NPWT) system is indicated for patients who would benefit from a suction device (NPWT) as it creates an environment that promotes wound healing by secondary or tertiary (delayed primary) intention by preparing the wound bed for closure, reducing edema, promoting granulation tissue formation and perfusion, and by removing exudate and infectious material.
Where it was distributed
US Nationwide Distribution domestically to AR, CA, FL, GA, IL, IN, LA, MI, MN, MO, NC, NJ, NY, OH, OK, PA, TX. Distributed internationally to Spain, Italy, Denmark, Sweden, Switzerland, Netherlands.
Nationwide ArkansasCaliforniaFloridaGeorgiaIllinoisIndianaLouisianaMichiganMinnesotaMissouriNorth CarolinaNew JerseyNew YorkOhioOklahomaPennsylvaniaTexas
Questions about this recall
Is Invia Motion Negative Pressure Wound Therapy System recalled?
Yes. Medela recalled Invia Motion Negative Pressure Wound Therapy System on 7 Feb 2018. The recall is Class II and its status is Terminated. Recall number Z-2528-2018.
Why was it recalled?
Device may display a battery missing error.
Which lots are affected?
a. Endure Negative Pressure Wound Therapy (Expected life 3 years); b. 15 Days Negative Pressure Wound Therapy (Expected life 15 days); c. 60 Days Negative Pressure Wound Therapy (Expected life 60 days); d. Endure Negative Pressure Wound Therapy (Expected life 3 years); e. 15 Days Negative Pressure Wound Therapy (Expected life 15 days); f. 60 Days Negative Pressure Wound Therapy (Expected life 60 days). Serial No. 1670458 1670488; 1670490; 1670492; 1670496 1670512; 1675368 1675419; 1675421 1675431; 1675433 1675443; 1675449; 1676316 1676365; 1676662 1676709; 1676711; 1676713; 1676715; 1676718 - 1676753; 1676755 1676756; 1676758 1676759; 1676762 1676861; 1677718 1677767; 1679752 1679765; 1679767 1679851; 1689658 1689757; 1696087 1696088; 1696095 1696111; 1696113 1696136; 1696356 1696455; 1697916 1697965; 160884 885; 1660887; 1660894 895; 1660901 903; 1660907; 1660915; 1660918 919; 1660921 22; 1660929; 1660934 935; 1660937; 1660940; 1660953; 1660955; 1660957 959; 1660961 963; 1660966; 1660969; 1660977 980; 1660986; 1660988; 1660991 998; 16611001 002; 1661005; 1661013 014; 1661018; 1661020; 1661032; 1661042; 1661052; 1661055; 1661062; 1661064; 1661066; 1661069; 1661076; 1661078; 1661081; 1661083; 1661086; 1661090; 1661092; 1661094 096; 1661099 112; 1661115; 1661117; 1661122; 1661123; 1662223; 1662230; 1662233; 1662237; 1662241 243; 1662245; 1662247 248; 1662252; 1662255 260; 1662263; 1662265 266; 1668362 369; 1668380 385; 1668392 394; 1668396 398; 1668402 403; 1668426; 1668430; 1668437; 1668441; 1668447; 1668451 452; 1668454 455; 1668458; 1668463; 1668466; 1668469; 1668473; 1668488; 1668494 495; 1668506 507; 1668512 515; 1668520 529; 1669591 593; 1669595 601; 1670635; 1670638; 1670641 642; 1670683 689; 1670694; 1670696; 1670698 706; 1670997; 1660883 884; 1660886; 1660888 893; 1660895 900; 1660904 906; 1660908 914; 1660916 917; 1660920; 1660923 933; 1660936 952; 1660954; 1660956; 1660960; 1660964 965; 1660967; 1660974 976; 1660981 984; 1660986 987; 1661000; 1661010; 1661021; 1661029; 1661036; 1661040; 1661049; 1661056; 1661060; 1661065; 1661073; 1661080; 1661084 085; 1661087; 1661089; 1661091; 1661093; 1661095; 1661097 098; 1661100 116; 1661118 121; 1661123 124; 1662225; 1662227; 1662232; 1662234; 1662236; 1662238 240; 1662244; 1662249 250; 1662253 254; 1662261 262; 1662264; 1668350; 1668375 376; 1668379; 1668386 387; 1668389 391; 1668395; 1668399 401; 1668405; 1668407 408; 1668410 416; 1668418 419; 1668421 425; 1668427; 1668432 439; 1668443 445; 1668447; 1668449; 1668453; 1668456 457; 1668459 462; 1668467 468; 1668471; 1668474; 1668481; 1668484; 1668492 494; 1668496 497; 1668501 502; 1668509 510; 1668514; 1668516 517; 1668520; 1668522;
Where was it sold?
US Nationwide Distribution domestically to AR, CA, FL, GA, IL, IN, LA, MI, MN, MO, NC, NJ, NY, OH, OK, PA, TX. Distributed internationally to Spain, Italy, Denmark, Sweden, Switzerland, Netherlands.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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