LifeScan OneTouch SureSoft Lancing Device, single use lancing device.
FDA device recall Z-0271-06 · posted 2005-12-08 · Terminated
Recall details
- Recalling firm
- Lifescan Inc
- Reason for recall
- In some cases, the needles in the single use lancing device may not retract, causing a potential for needle sticks.
- Action taken
- 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.
- Root cause
- Other
- Status
- Terminated
- Product code
- NBW
- Quantity affected
- 1123 boxes
- Distribution
- Product was distributed to a total of 21 direct consignees and 45 end-user customers, for a total of 66 consignees in both the US and canada.
- Date initiated
- 2005-10-11
- Date posted
- 2005-12-08
- Date terminated
- 2006-11-21
- Location
- Milpitas, CA
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