Atlas FDA

Ultracell Classic Anatomical Nasal Packing w/Tube (pediatric) Catalog # 10126-CT

FDA device recall Z-0479-03 · posted 2003-01-30 · Terminated

Recall details

Recalling firm
Ultracell Medical Technologies
Reason for recall
Sterility of the device is compromised
Action taken
Ultracell Medical Technologies initiated the recall by fax or mail on 1/8/03. The firm requested return of product . Distributors were requestd to recall to their accounts.
Root cause
Other
Status
Terminated
Product code
EMX
Quantity affected
6 boxes
Distribution
Nationwide
Date initiated
2003-01-08
Date posted
2003-01-30
Date terminated
2012-05-01
Location
North Stonington, CT

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