Stryker Instruments Div. of Stryker Corporation Stryker Advanced Cement Mixer (ACM) Bowl and Base without 180 Gram Cement Cartridge for use with Stryker High Vacuum Cement Injection System, sterile; REF 306-554, Stryker Instruments, Kalamazoo, MI 49001. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stryker Advanced Cement Mixer (ACM) Bowl and Base without 180 Gram Cement Cartridge for use with Stryker High Vacuum Cement Injection System, sterile; REF 306-554, Stryker Instruments, Kalamazoo, MI 49001.
Brand
Stryker Instruments Div. of Stryker Corporation
Lot Codes / Batch Numbers
Lot Numbers: 05167CG2, 05192012, 05223012 and 06335012.
Products Sold
Lot Numbers: 05167CG2, 05192012, 05223012 and 06335012.
Stryker Instruments Div. of Stryker Corporation is recalling Stryker Advanced Cement Mixer (ACM) Bowl and Base without 180 Gram Cement Cartridge for use with Str due to Sterility may be compromised, as the packaging may have channels in the packaging seal.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sterility may be compromised, as the packaging may have channels in the packaging seal.
Recommended Action
Per FDA guidance
Stryker notified consignees via Medical Device Recall Notification letter dated 1/10/08 to quarantine the product and to return it.
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