Device recall

Z-2036-2018: AmerisourceBergen PF Latex SG (Surgical Glove), Sterile, Powder Free, Size 6.5…

FDA device recall · Class II · WRP Asia Pacific Sdn Bhd

Key facts

Recall number (Z-number) Z-2036-2018
Recall event 79992
Product AmerisourceBergen PF Latex SG (Surgical Glove), Sterile, Powder Free, Size 6.5, Item No. 10112
Product code KGO
Recalling firm WRP Asia Pacific Sdn Bhd
Recall class Class II
Status Terminated
Termination date May 30, 2019
510(k) numbers K020019
FEI number 3002808507

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)