Device recall

Z-1116-2014: DROP-ARM CONVALESCENT RECLINER 5271/5281 with One-touch release for drop-arms…

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

Key facts

Recall number (Z-number) Z-1116-2014
Recall event 67377
Product DROP-ARM CONVALESCENT RECLINER 5271/5281 with One-touch release for drop-arms, Built-in headrest, Padded push-handle, Three-position lock, Over-lap tray. The products are a multi position recliners with a steel frame used primarily in long term care or convalescent facilities. The recliners are…
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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