Device recall

Z-1117-2014: XL CONVALESCENT RECLINER 5291/529S with Padded armrests with guard, Dual fold…

FDA device recall · Class II · Winco Mfg., LLC

Key facts

Recall number (Z-number) Z-1117-2014
Recall event 67377
Product XL CONVALESCENT RECLINER 5291/529S with Padded armrests with guard, Dual fold down side-tables, Removable side panels, Built-in head-rest. The products are a multi position recliners with a steel frame used primarily in long term care or convalescent facilities. The recliners are suitable as general…
Product code INM
Recalling firm Winco Mfg., LLC
Recall class Class II
Status Terminated
Termination date Dec 30, 2014
FEI number 1027229

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

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