Safety Lancet for capillary blood sampling, 1.6 mm x 28G, Mini, Sarstedt. (Blood lancet)
FDA Recall Z-0114-2009 · Posted 2008-10-14
Recalling FirmSarstedt Inc
Recall StatusTerminated
Product CodeFMK
Date Initiated2008-08-27
Date Terminated2012-04-24
Product Quantity1000 pieces
Reason for Recall
The product from this lot may not retract the lancet into the safe position inside the lancet body after the trigger is actuated.
Firm Action
The consignee was notified via letter that was hand delivered on 08/27/2008. All of the distributed product was picked up from the consignee and returned to Sarstedt, Inc. None of the product had been used. All action was completed on 8/27/2008. Contact Sarstedt at 1-828-465-4000 for assistance.
Root Cause
Process control
Distribution Pattern
NC
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.