ClearanceBrief
Recall Z-1084-2007 ยท GDF Guide, Needle, Surgical

Synovis Surgical Inovation Div. of

Allez Medical Applications, Inc. 4Closure Surgical Fascia Closure System , Catalog ref. 4-23DGPS . Sterile, One Time Use, Contents 4 sets 1- suture passer instrument, 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 Universi

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.
Quantity34 boxes (136 units)
DistributionNationwide.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.