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Terminated

Genzyme Biosurgery Essentials Kit, Item Number 82004

FDA Recall Z-2310-2010 · Posted 2010-08-28

Recalling FirmGenzyme Corporation
Recall StatusTerminated
Product CodeLRO
Date Initiated2010-07-13
Date Terminated2012-01-30
Product Quantity3132 kits

Reason for Recall

Revised Labeling of Carticel Essentials Kit clarifies the non-sterile packaging of the outer clear plastic tray which should not be opened in the sterile field.

Firm Action

Genzyme notiifed physicians with the Dear Doctor letter on July 13, 2010 via UPS Ground delivery. The letter informed healthcare workers of the recent incidents and advise them to heed the Essentials Kit label and exercise proper handling of the Kit.. A fax return form will be provided for the physician to sign and return to Genzyme to acknowledge receipt of the notification. Contact Genzyme Medical Information at 800-453-6948, option #3 for any additional information or contact your Genzyme sales representative with any questions.

Root Cause

Labeling design

Distribution Pattern

Nationwide

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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