Stryker Endoscopy Stryker brand Insufflation Tube Set and High Flow Insufflation Tube Set, Model Numbers: 620-030-201, 620-030-301 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stryker brand Insufflation Tube Set and High Flow Insufflation Tube Set, Model Numbers: 620-030-201, 620-030-301
Brand
Stryker Endoscopy
Lot Codes / Batch Numbers
Lots 04051142--06121FE2, 04051142--06123FE2
Products Sold
Lots 04051142--06121FE2, 04051142--06123FE2
Stryker Endoscopy is recalling Stryker brand Insufflation Tube Set and High Flow Insufflation Tube Set, Model Numbers: 620-030- due to Device for which sterility may be compromised as evidenced by a loss of package integrity.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Device for which sterility may be compromised as evidenced by a loss of package integrity.
Recommended Action
Per FDA guidance
On 6/2/06, the firm initiated the recall and its notification was via letters explaining the reason for the recall and requesting the product be returned.
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