Device recall

Z-1244-2009: TEVADAPTOR Closed Drug Reconstitution and Transfer System, a closed system used…

FDA device recall · Class II · Migada Inc.

Key facts

Recall number (Z-number) Z-1244-2009
Recall event 51421
Product TEVADAPTOR Closed Drug Reconstitution and Transfer System, a closed system used to prepare drugs, including cytotoxic drugs, for intravenous infusion or injection. Model number is MG412110. The device is a single use device.
Product code LHI
Recalling firm Migada Inc.
Recall class Class II
Status Terminated
Termination date Jul 27, 2009
510(k) numbers K051669, K071741
FEI number 3002807615

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

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