Axya Medical Axya Anchor, 5.0 mm Titanium in Super Kit, Catalog Number: CAT1270, Axya Medical, Inc., Beverly, MA 01915 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Axya Anchor, 5.0 mm Titanium in Super Kit, Catalog Number: CAT1270, Axya Medical, Inc., Beverly, MA 01915
Brand
Axya Medical
Lot Codes / Batch Numbers
Lot Numbers: 203415, 203445, 203588, 203604, 203739, 203742, 203791, 203798, 203820, 203823, 203834, 203863, 203905, 203915, 203994, 204025, 204126, 204176, 204187, 204199, 204209, 204239, 204246, 204277, 204302, 204308, 204350, 204355, 204390, 204459, 204482, 204511, 204513, 204516, 204521, 204546, 204626, 204642, 204646, 204651, 204673, 204692, 204721, 204736, and 204781
Products Sold
Lot Numbers: 203415, 203445, 203588, 203604, 203739, 203742, 203791, 203798, 203820, 203823, 203834, 203863, 203905, 203915, 203994, 204025, 204126, 204176, 204187, 204199, 204209, 204239, 204246, 204277, 204302, 204308, 204350, 204355, 204390, 204459,204482, 204511, 204513, 204516, 204521, 204546, 204626, 204642, 204646, 204651,204673, 204692, 204721, 204736, and 204781
Axya Medical is recalling Axya Anchor, 5.0 mm Titanium in Super Kit, Catalog Number: CAT1270, Axya Medical, Inc., Beverly, MA due to Sterility Compromised (Package Integrity): Sterility of the device may be compromised due to holes in the sterile packaging. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sterility Compromised (Package Integrity): Sterility of the device may be compromised due to holes in the sterile packaging
Recommended Action
Per FDA guidance
Axya Medical notified customers by letter, Urgent-Product Recall, dated 9/25/07 , via UPS . Users are requested to return product and complete the reply form.
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