Stryker Howmedica Osteonics T2 Tibia Nail, Standard 9 x 300 mm, T2 Tibia System, Catalog No. 1822-0930S. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
T2 Tibia Nail, Standard 9 x 300 mm, T2 Tibia System, Catalog No. 1822-0930S.
Brand
Stryker Howmedica Osteonics
Lot Codes / Batch Numbers
Lot K884459
Products Sold
Lot K884459
Stryker Howmedica Osteonics is recalling T2 Tibia Nail, Standard 9 x 300 mm, T2 Tibia System, Catalog No. 1822-0930S. due to The device does not have an oblong hole for dynamic locking as required.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The device does not have an oblong hole for dynamic locking as required.
Recommended Action
Per FDA guidance
Product recall letters and Product accountability forms were sent via FedEx on 8/4/2003 with return receipt.
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 noticeDistribution
As reported by FDA
CA, GA, IN, KS, PA, VA
Page updated: Jan 10, 2026