ClearanceBrief
Recall Z-0649-2012 ยท GAM Suture, Absorbable, Synthetic, Polyglycolic Acid

Mani, Inc. - Kiyohara Facility

MANI Needle and Suture Pack, 8-0 PGA Absorbable, Model 2090, 30 cm suture and needle, packaged in individual aluminum pack, within tyvek packaging, 12 packages per box, and labeled in part ***Mani, Inc 8-3 Kiyohara Industrial Park Utsunomiya, Tochigi, Japan*** For use in short term soft tissue approximation, including use in ophthalmic surgery, but not for use in cardiovascular and neurological

DateJan 11, 2012 (initiated Jul 20, 2011)
StatusTerminated
ReasonSurgical sutures may be weak and may not function as intended during surgical procedures.
Root causeComponent change control
ActionThe manufacturer notified consignees by phone, via fax with a letter, and e-mail on 07/20/11. The letter asked customers to check their inventory for any of the affected product, and if they had any product remaining to place the amount in the list "Returned." If there was no product left, then the amount used should be placed in the list "Used." Customers needed to complete and sign the document, being sure to send it and any remaining product to the address provided. Credit would be issued once goods were received. If customers have questions, they should contact the firm.
Quantity497 boxes
DistributionNationwide Distribution -- PA and FL.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K053636MANI NEEDLE & SUTURE PACK (PGA ABSORBABLE)
Mani, Inc., Mar 14, 2006