Device recall

Z-0152-04: 100 inch (254 cm) 15 Drop Administration Set with FlowSafe Flow Controller and…

FDA device recall · Class II · Maximus Medical Products Inc

Key facts

Recall number (Z-number) Z-0152-04
Recall event 27697
Product 100 inch (254 cm) 15 Drop Administration Set with FlowSafe Flow Controller and Max Y Connector, 50 per box. Product No. MFS102
Product code FPA
Recalling firm Maximus Medical Products Inc
Recall class Class II
Status Terminated
Termination date Nov 25, 2003
FEI number 3003698179

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 1,000+ 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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