Device recall

Z-0264-04: CX9625 Light Pipe (25 Gauge). The product is sold in packs containing six pipes.

FDA device recall · Class II · Bausch & Lomb Inc

Key facts

Recall number (Z-number) Z-0264-04
Recall event 27714
Product CX9625 Light Pipe (25 Gauge). The product is sold in packs containing six pipes.
Product code HJM
Recalling firm Bausch & Lomb Inc
Recall class Class II
Status Terminated
Termination date Apr 5, 2004
510(k) numbers K940393
FEI number 1317628

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

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