Device recall

Z-1946-2014: Name: Pasteur Pipets, used by the embryologist in the IVF Laboratory. Model…

FDA device recall · Class II · ORIGIO, Inc

Key facts

Recall number (Z-number) Z-1946-2014
Recall event 68592
Product Name: Pasteur Pipets, used by the embryologist in the IVF Laboratory. Model numbers: PP-5.75-90 PP-9-90 PP-5.75-90PL PP-9-90PL
Product code MQK
Recalling firm ORIGIO, Inc
Recall class Class II
Status Terminated
Termination date Jul 20, 2015
510(k) numbers K000915
FEI number 1216677

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

Browse all FDA device recalls (products)