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FDAFDA · Food and drugs·Recall number Z-1656-2013

ARGENT SURGICAL SYSTEMS***BIOPSY Punches*** Disposable manual instrument for skin biopsy.

Published July 10, 2013 · Recall initiated: March 18, 2013

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Due to lack of sterilization.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Clorox Healthcare Holdings, LLC (dba HealthLink)
Distributor
Worldwide Distribution-USA (nationwide) including Puerto Rico and the states of AZ, CA, CO, FL, GA, IA, IL, IN, MI, MO, MS, MT, NC, NJ, NY, OH, SC,TX ,VA ,WA, WI, and HI, and the countries of Canada, Mexico, and New Zealand.
Lot
1232040, 1232039, 1232038, 1232037, 1232029, 1232027, 1232026, 1232025, 1232023, 1232022, 1232019, 1232018, 1232017, 1232016, 1232014, 1232012, 1232011, 1232008, 1232007, 1232006, 1231322, 1231321, 1231320, 1231315, 1226439, 1226438, 1226434, 1226433, 1226431, 1226430, 1226429, 1226428, 1226427, 1226426, 1226422, 1226420, 1226419, 1226418, 1226417, 1226415, 1226414, 1222301, 1222302, 1222303, 1222304, 1222305, 1222306, 1222307, 1222308, 1222309, 1222310, 1222311, 1222312, 1222313, 1222314, 1222315, 1222316, 1222317, 1222323, 1222324, 1222325, 1222326, 1222327, 1222328, 1222329, 1222330, 1222331, 1222332, 1222333, 1222334, 1222335, 1222336, 1222337, 1222338, 1222339, 1222001, 1217408, 1217407, 1217406, 1217405, 1217403, 1217402, 1217401, 1214505, 1213925, 1213922, 1213920, 1213919, 1213915, 1213914, 1213913, 1213912, 1213911, 1213909, 1213908, 1213904, 1213903, 1213902, 1213901, 1211614, 1211613, 1208728, 1208727, 1208726, 1208725, 1208724, 1208723, 1208722, 1208721, 1208720, 1207323, 1205328, 1205327, 1205326, 1205325, 1205324, 1205323, 1205322, 1205321, 1205320, 1205319, 1205318, 1205317, 1205316, 1205315, 1201925, 1201924, 1201923, 1201922, 1201921, 1201920, 1201919, 1201918, 1201917, 1201916, 1201915, 1201914, 1201913, 1201912, 1201911, 1201910, 1201909, 1200511, 1200319, 1134635, 1134634, 1134633, 1134632, 1134631, 1134630, 1134629, 1134628, 1134627, 1134626, 1134625, 1134624, 1129718, 1129329, 1129326, 1129325, 1129323, 1129322, 1129321, 1129320, 1129319, 1129318, 1129317, 1129316, 1129315, 1129314, 1128318, 1125622, 1125621, 1125620, 1125619, 1125618, 1125617, 1125616, 1125615, 1123516, 1123515, 1123514, 1123010, 1122921, 1122920, 1122919, 1122918, 1122917, 1122916, 1122915, 1122719, 1122718, 1122717, 1122716, 1121520, 1121519, 1121518, 1121517, 1121516, 1121515, 1120814, 1120727, 1120726, 1120725, 1120724, 1120723, 1120722, 1120721, 1120720, 1119923, 1119922, 1119921, 1119920, 1119919, 1119324, 1119323, 1119322, 1119321, 1119320, 1119319, 1118723, 1118722, 1118721, 1118720, 1118719, 1118718, 1118717, 1118716, 1118024, 1118023, 1118022, 1118021, 1118020, 1118019, 1118018, 1118017, 1118016, 1117410, 1117409, 1117408, 1117407, 1116714, 1116713, 1116712, 1116711, 1116710, 1116709, 1116418, 1116018, 1116017, 1116016, 1116015, 1116014, 1116013, 1113217, 1113216, 1112221, 1111807, 1111806, 1111805, 1111804, 1111518, 1111021, 1111020, 1111019, 1111018, 1111017, 1111016, 1110129, 1110128, 1110127, 1110126, 1110125, 1110124, 1110123, 1110122, 1109619, 1109618, 1109616, 1109018, 1109017, 1109016, 1109015, 1109014, 1108315, 1108314, 1108313, 1108312, 1108310, 1108309, 1108025, 1108024, 1108023, 1108022, 1108021, 1108020, 1106226, 1106225, 1105422, 1104210, 1104209, 1104208, 1104207, 1103919, 1102417, 1101819, 1101818, 1101817, 1101816, 1101815, 1100315, 1036135, 1036134, 1036133, 1036132, 1036131, 1036130, 1036129, 1036128, 1036126, 1036125, 1036124, 1036123, 1007711.
Risk classification
Class II
Area (FDA)
device
Country
United States

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