Stryker Instruments Div. of Stryker Corporation Stryker Instruments 2.1 mm Cross-Cut Fissure Bur, carbide extended, sterile; REF 2296-101-621. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stryker Instruments 2.1 mm Cross-Cut Fissure Bur, carbide extended, sterile; REF 2296-101-621.
Brand
Stryker Instruments Div. of Stryker Corporation
Lot Codes / Batch Numbers
Lots 08311017 and 08336027.
Products Sold
Lots 08311017 and 08336027.
Stryker Instruments Div. of Stryker Corporation is recalling Stryker Instruments 2.1 mm Cross-Cut Fissure Bur, carbide extended, sterile; REF 2296-101-621. due to The cross-cuts are missing on the device, which will result in poor cutting and overheating and/or smoking of the device.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The cross-cuts are missing on the device, which will result in poor cutting and overheating and/or smoking of the device.
Recommended Action
Per FDA guidance
Consignees were notified by letter dated 10/5/09 and requested to return the devices to Stryker. The international account was notified by email.
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, LA, OH, WI
Page updated: Jan 10, 2026