FDA Recall Terminated

Monomid Non-Absorbable Suture are blue, monofilament synthetic absorbable suture, with different sizes and different needle sizes. The products are labeled in parts. These sutures are intended for use in general soft tissue approximation and/or ligation including use in cardiovascular, ophthalmic, and neurological surgery.

Recall: Z-3177-2011 · Initiated June 29, 2011

Recall

Recall Number
Z-3177-2011
Event Number
59759
Firm
C P Medical Inc.
FEI Number
3002609049
Product Code
GAR
Status
Terminated
Root Cause
Process control
Initiated
June 29, 2011
Posted
September 9, 2011
Terminated
May 24, 2012
Address
803 NE 25th Avenue, Portland, OR, 97232-2304

Description

Monomid Non-Absorbable Suture are blue, monofilament synthetic absorbable suture, with different sizes and different needle sizes. The products are labeled in parts. These sutures are intended for use in general soft tissue approximation and/or ligation including use in cardiovascular, ophthalmic, and neurological surgery.

Reason

Unapproved dye was used in manufacturing the non-absorbable blue nylon suture material.

Action

CP Medical sent a "RECALL NOTICE" letter dated June 29, 2011 to all affected customers. The letter describes the product, problem, and actions to be taken by the customers. The letter instructs customers to discontinue use of the affected products in the human market and to return all their existing stock. A Recall Checklist was enclosed for customers to complete and return. Contact Customer Service at 1-800-950-2763 for a Return Good Authorization and shipping account number. The firm will pay for shipping cost and replace product at no cost to customers.

Distribution

Worldwide Distribution-USA (nationwide) and the countries of Italy, Romania, South Africa, and Taiwan.

Quantity

776 dozens boxes