—#41711

Product

Custom Procedure Trays, containing various configurations of medical and surgical devices, packed in plastic pouches, labeled in part ***Avid Medical, The custom procedure tray company Toano, Virginia 23168***Sterile~Disposable~Single Use Only***, and further identified by the following catalog numbers: BOOZ001-01 CATARACT PACK*** VMLR0009-05 FEM POP*** AZSS001-01 SINGLE SHOT EPIDURAL TRAY*** META026-01 SHOULDER*** MPOC002-02 ARTHROSCOPY PACK*** MMMC002 UNIVERSAL ARTHROSCOPY PACK*** ORHS023-03 OBSTETRICAL PACK W/POUCH*** MSCB002-02 BASIC PACK*** ADVH002-08 OPEN HEART KLICH PACK*** ADVM005-02 PACEMAKER-IL MASONIC*** CILS004-03 EXTREMITY PACK*** NOIN004 ARTHROGRAM PACK*** RMRI036-11 TOTAL JOINT PACK*** NRSC0003-06 ARTHROSCOPY PACK*** AV10584-03 COMMUNITY RETINAL DETACHMENT*** STJN030-02 HEART DRAPE TRAY*** STJN045 HEART OFF PUMP*** PHLS008-04 SPECIAL PROCEDURES PACK*** UHSN035-02 TOTAL KNEE*** SLIZ004a-02 CATH TRAY*** NYOD008 Abdominal Preservation Kit*** NYOD011 PEDIATRIC ABDOMINAL*** FAMC017-05 MAJOR BASIN SET*** AGAK005-04 BASIN SET-SURGERY CENTER*** AV010773-02 C-SECTION PACK*** OSUM018-04 OPHTHALMOLOGY CUSTOM TRAY*** KENT005-01 CAROTID*** HVCCA-10 HEART PACK*** SUMM004-04 Harris Basic*** MCVA0020-07 BUNDLE, EYE*** MCVA0025-04 BUNDLE, LOWER EXTREMITY*** MCVA0033-06 PDS, MAJOR EAR*** MCVA0039-06 PDS, TOTAL KNEE*** MCVA0044-02 PACEMAKER PACK*** NAPO0014-04 LAP CHOLE CUSTOM TRAY*** NAPO0025-05 HAND & PODIATRY TRAY*** NAPO0061-02 ABDOMINOPLASTY CUSTOM TRAY*** LIFE0027-06 C.V. TRANSPORT BOX*** WIAS002-01 UNIVERSAL BLOCK TRAY*** UMCW013-07 TOTAL KNEE PDS***

FDA product code: LRO — General Surgery Tray
Device class: Class 2
Medical specialty: General, Plastic Surgery
Affected lot / code info: Lots: 385569 386370 388085 380910 385604 386873 386153 388558 387906 386224 385726 386714 386721 386142 387590 386731 386732 386337 385262 386756 383386 383385 385819 386706 385980 386074 386472 385660 386649 386409 384525 386543 386410 385493 386849 385945 387453 386357 388777 385542

Why it was recalled

Defect in packaging of medical devices may compromise sterility of these products used in medical and surgical procedures.

Root cause (FDA determination)

Other

Action the firm took

The recalling firm notified distributors and end users by letter 09/07/05. The notification advised of product packaging in which seal integrity may have been compomised. The recall letter lists specific lots and item numbers of the custom trays to be returned for replacement or reimbursement. A response form is included in the notification.

Recalling firm

Firm: Avid Medical Inc
Address: 9000 Westmont Drive, Stonehouse Commerce Park Toano, Virginia 23168

Distribution

Distribution pattern: The product was sold to distributors and end user medical facilities nationwide.

Timeline

Recall initiated: 2005-09-09
Posted by FDA: 2005-09-14
Terminated: 2006-05-08
Status: —

Source: openFDA Device Recall endpoint. Recall record ID #41711. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.