ClearanceBrief
Recall Z-1083-2007 ยท GDF Guide, Needle, Surgical

Synovis Surgical Inovation Div. of

Allez Medical Applications, Inc. 4Closure Surgical Fascia Closure System , Catalog ref. 4-23DG. Sterile, One Time Use, Contents 4 sets 1-guide rod, 23 mm, 250 mm long, dilating. Distributed by Aliez Medical Applications, Inc., Santa Ana, CA 92707. Synovis over labels the "Distributed by....", For Customer Service Contact: Synovis Surgical Innovations 2575 University Ave W., St. Paul, MN 55114-1

DateJul 24, 2007 (initiated Jun 19, 2007)
StatusTerminated
ReasonThere is a potential for the pouch to become damaged during shipping, compromising the sterility of the device inside.
Root causeOther
ActionConsignees were sent a letter on June 19, 2007. The letter identified the product and problem. The letter also included a form for inventory purposes which is to be completed and faxed to Synovis.
Quantity19 boxes ( 76 units)
DistributionNationwide.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.