Device recall

Z-0281-04: Pediatric Air Aspirator Needle manufactured by Novosci Corp., The Woodlands, TX

FDA device recall · Class II · Novosci Corp

Key facts

Recall number (Z-number) Z-0281-04
Recall event 27783
Product Pediatric Air Aspirator Needle manufactured by Novosci Corp., The Woodlands, TX
Product code GAA
Recalling firm Novosci Corp
Recall class Class II
Status Terminated
Termination date Apr 12, 2004
510(k) numbers K801393
FEI number 1625519

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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