FDA recall record

Ethicon EVARREST Fibrin Sealant Patch, Manufactured by: Omrix Biopharmaceuticals, Ltd recall — FDA Z-1996-2016

Ethicon is recalling EVARREST Fibrin Sealant Patch because the characters "0-bad" were printed in the expiration date field on the foil pouch labels of…

Class IIclassification
Z-1996-2016official record ID
Jun 22, 2016report date

Recall record at a glance

Official recordZ-1996-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmEthicon, Inc.
Report dateJun 22, 2016
Recall initiation dateApr 11, 2016
Quantity228 units
LocationSomerville, NJ, United States

Official product description

EVARREST Fibrin Sealant Patch, Manufactured by: Omrix Biopharmaceuticals, Ltd, Israel. Indicated for use with manual compression as an adjunct to hemostasis for control of bleeding during adult liver surgery and soft tissue bleeding in adults when control of bleeding by standard surgical methods of hemostasis is ineffective or impractical.

Why the product was recalled

Ethicon is recalling EVARREST Fibrin Sealant Patch because the characters "0-bad" were printed in the expiration date field on the foil pouch labels of the Fibrin Patch units instead of the valid expiration date (2016-12-28).

Distribution information

Nationwide Distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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