Device recall

Z-1234-06: 3M Nexcare First Aid High Performance Gauze Pad. Individually wrapped & sterile…

FDA device recall · Class II · 3M Company / Medical Division

Key facts

Recall number (Z-number) Z-1234-06
Recall event 34633
Product 3M Nexcare First Aid High Performance Gauze Pad. Individually wrapped & sterile. catalog # 434-10. 3M Consumer Health Care, St. Paul, MN 55144-1000. Made in USA. UPC 05113166774.
Product code FRL
Recalling firm 3M Company / Medical Division
Recall class Class II
Status Terminated
Termination date Jan 5, 2007
FEI number 2110898

At a glance

  • None 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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