Device recall

Z-0824-06: Hobbs Medical 3 Prong Looped Retriever, a disposable device to be used by…

FDA device recall · Class II · Hobbs Medical, Inc.

Key facts

Recall number (Z-number) Z-0824-06
Recall event 35011
Product Hobbs Medical 3 Prong Looped Retriever, a disposable device to be used by physician to remove foreign object or cauterize polyp specimens from the GI tract. REF: 5030 and 5030S
Product code KOG
Recalling firm Hobbs Medical, Inc.
Recall class Class II
Status Terminated
Termination date Jun 27, 2006
510(k) numbers K833125
FEI number 1220592

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 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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