Device recall

Z-0876-2021: Reliance Vision Single-Chamber Washer/Disinfector - Product Usage: intended for…

FDA device recall · Class II · Steris Corporation

Key facts

Recall number (Z-number) Z-0876-2021
Recall event 86937
Product Reliance Vision Single-Chamber Washer/Disinfector - Product Usage: intended for use in the cleaning and intermediate level disinfection of soiled reusable utensils, trays, glassware, bedpans and urinals, rubber and plastic goods, simple hard-surfaced rigid surgical instruments, such as forceps and…
Product code MEC
Recalling firm Steris Corporation
Recall class Class II
Status Terminated
Termination date Jun 21, 2022
FEI number 1527821

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

Browse all FDA device recalls (products)