Device recall

Z-1109-2017: Cryptococcal Antigen Lateral Flow Assay (CrAg LFA), Reference # CR2003

FDA device recall · Class II · Immuno-Mycologics, Inc

Key facts

Recall number (Z-number) Z-1109-2017
Recall event 76159
Product Cryptococcal Antigen Lateral Flow Assay (CrAg LFA), Reference # CR2003
Product code GMD
Recalling firm Immuno-Mycologics, Inc
Recall class Class II
Status Terminated
Termination date Mar 8, 2017
510(k) numbers K112422
FEI number 1627497

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 1–9 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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