Lifescan Inc LifeScan OneTouch SureSoft Lancing Device, single use lancing device. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
LifeScan OneTouch SureSoft Lancing Device, single use lancing device.
Brand
Lifescan Inc
Lot Codes / Batch Numbers
Part Number 021-139-01 OT SureSoft Hospital, Regular 200, Lot numbers, SW2764, SW3427, SW2779, SW2785, SW3339, SW3342, SW3394, SW3395. Part number 021-140-01, OT SureSoft Hospital, Gentle 200, Lot numbers, SW2846, SW2833, SW2774, SW2868, SW2834, SW2765, SW2869, SW2894, SW2896.
Products Sold
Part Number 021-139-01 OT SureSoft Hospital, Regular 200, Lot numbers, SW2764, SW3427, SW2779, SW2785, SW3339, SW3342, SW3394, SW3395. Part number 021-140-01, OT SureSoft Hospital, Gentle 200, Lot numbers, SW2846, SW2833, SW2774, SW2868, SW2834, SW2765, SW2869, SW2894, SW2896.
Lifescan Inc is recalling LifeScan OneTouch SureSoft Lancing Device, single use lancing device. due to In some cases, the needles in the single use lancing device may not retract, causing a potential for needle sticks.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
In some cases, the needles in the single use lancing device may not retract, causing a potential for needle sticks.
Recommended Action
Per FDA guidance
On October 11, 2005, 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 noticeDistribution
As reported by FDA
IN
Page updated: Jan 10, 2026