Device recall

Z-1141-2021: Slush + Warmer Disc Drape; Model ORS-320 Slush + Warmer Disc Drapes - Product…

FDA device recall · Class II · Ecolab Inc

Key facts

Recall number (Z-number) Z-1141-2021
Recall event 87173
Product Slush + Warmer Disc Drape; Model ORS-320 Slush + Warmer Disc Drapes - Product Usage: single-use equipment cover intended for use during various surgeries where warm irrigation, slush and/or cold solution is required.
Product code PUI
Recalling firm Ecolab Inc
Recall class Class II
Status Terminated
Termination date Jan 9, 2023
FEI number 3014342658

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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