Data Foundry

Medical device recalls 2016

Invacare¿ Foot Section for Semi & Full Electric Beds — Class II medical device recall Z-2401-2016

Terminated recall by Invacare Corporation, reported 2016-08-17, distributed nationwide. The firm recently identified a quality issue with the Junction box used in the Invacare Bariatric Bed. They di

Recall numberZ-2401-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmInvacare Corporation, Elyria, OH, United States
Recall initiated2016-03-15
Classified2016-08-11
Reported by FDA2016-08-17
Terminated2017-09-15
DistributedNationwide (US)
Countries outside the USCA
Quantity3,050 units
Serial numbers14LF046072, 15AF009530, 15AF009531, 15AF016194, 15AF016195, 15AF016196, 15AF016197, 15AF016198, 15AF022202, 15AF022206, 15AF034667, 15AF034669, 15AF034671, 15AF048735, 15AF048736, 15AF048737, 15AF048738, 15AF048739, 15AF048740, 15AF048741, 15AF048742, 15AF048743, 15AF048744, 15AF048745, 15AF048746 and 361 more
Model numbersBAR5490IVC

Product

Invacare¿ Foot Section for Semi & Full Electric Beds, Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.

Reason for recall

The firm recently identified a quality issue with the Junction box used in the Invacare Bariatric Bed. They discovered that the Junction Box may omit sparks which could result in a fire in the presence of flammable materials.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2401-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.