Device recall

Z-0011-2011: MAQUET HLM Tubing set with Bioline Coating (BEQ-TOP 21400 with 1/2 x 1/2 HG 0286…

FDA device recall · Class II · Maquet Inc.

Key facts

Recall number (Z-number) Z-0011-2011
Recall event 56728
Product MAQUET HLM Tubing set with Bioline Coating (BEQ-TOP 21400 with 1/2 x 1/2 HG 0286 Connector; Device Part Number BEQ-TOP 21400
Product code DWE
Recalling firm Maquet Inc.
Recall class Class II
Status Terminated
Termination date Sep 25, 2012
510(k) numbers K080592
FEI number 3008355164

At a glance

  • 1–9 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)