Stryker Instruments Div. of Stryker Corporation Stryker PainPump1.5 5-Day Infusion Kit; Product number 501-120-000. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stryker PainPump1.5 5-Day Infusion Kit; Product number 501-120-000.
Brand
Stryker Instruments Div. of Stryker Corporation
Lot Codes / Batch Numbers
Lots 2005053003 and 2005060301.
Products Sold
Lots 2005053003 and 2005060301.
Stryker Instruments Div. of Stryker Corporation is recalling Stryker PainPump1.5 5-Day Infusion Kit; Product number 501-120-000. due to The catheter tubing included in the kit may break during removal.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The catheter tubing included in the kit may break during removal.
Recommended Action
Per FDA guidance
Each consignee was notified of the recall via recall letter dated 2/7/06, which requested that they destroy the affected lots on site. International accounts were notified via 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 noticePage updated: Jan 10, 2026