Avid Medical Inc 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 ARTHROSC Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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 ARTHROSC
Brand
Avid Medical Inc
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
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
Avid Medical Inc is recalling Custom Procedure Trays, containing various configurations of medical and surgical devices, packed i due to Defect in packaging of medical devices may compromise sterility of these products used in medical and surgical procedures.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Defect in packaging of medical devices may compromise sterility of these products used in medical and surgical procedures.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026