FDA recall record

Ethicon Endo-Surgery HARMONIC ACE+ 7 Laparoscopic Shears with Advanced Hemostasis recall — FDA Z-0278-2016

Complaints of holes in Tyvek which can compromise the sterile barrier provided by the packaging.

Class IIclassification
Z-0278-2016official record ID
Nov 25, 2015report date

Recall record at a glance

Official recordZ-0278-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmEthicon Endo-Surgery Inc.
Report dateNov 25, 2015
Recall initiation dateSep 23, 2015
Quantity441,490 pieces
LocationBlue Ash, OH, United States

Official product description

HARMONIC ACE+ 7 Laparoscopic Shears with Advanced Hemostasis (23cm, 36cm, 45cm length), Ethicon Endo-Surgery. Indicated for soft tissue incisions when bleeding control and minimal thermal injury are desired.

Why the product was recalled

Complaints of holes in Tyvek which can compromise the sterile barrier provided by the packaging.

Distribution information

Distributed US (nationwide) including the District of Columbia & Puerto Rico and in the countries of ARUBA, AUSTRALIA, BELGIUM, BRAZIL, CANADA, CHILE, CHINA, COLOMBIA, ECUADOR, HONG KONG, INDIA, JAPAN, KOREA, MALAYSIA, MEXICO, PANAMA, PERU, PHILIPPINES, SINGAPORE, SINGAPORE, THAILAND, TAIWAN & VIETNAM.

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: Telephone.

What to do next

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