Reported Jul 4, 2012 · Terminated
Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R) ARROWgard Blue(R) Catheter Product Usage: The…
Arrow International Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Arrow International Inc · 2400 Bernville Road · Reading, PA · 19605
Is this the product you have?
- Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R) ARROWgard
- Blue(R) Catheter Product UsageThe multiple-lumen catheter permits venous access to central circulation
- Lot codes and dates
146 of 146 products
Products covered by this recall Model / number Product as published AD-24703-OBlots ZF1013508, ZF1024536, ZF1025079, ZF1036035, ZF1036449, ZF1057072, ZF1068314, ZF1079528, ZF1080288, ZF1080633, ZF1091019, ZF1092076, ZF1102574, ZF1124769, ZF1124963, ZF1125081, and ZF2016671. AD-24730-Elots ZF0111748, ZF0122465, ZF1013943, ZF1024429, ZF1035851, ZF1035852, ZF1046809, ZF1047095, ZF1056833, ZF1068324, ZF1068691, ZF1080036, ZF1080307, ZF1091021, ZF1102236, ZF1102876, ZF1113491, ZF1113853, ZF1114656, and ZF1125078. AD-24730-OBlots ZF0111749, ZF1013521, ZF1024545, ZF1035853, ZF1047096, ZF1056829, ZF1080032, ZF1091022, ZF1125298, ZF1125525, and ZF2016325. AD-24730-OLlots ZF1013523, ZF1024547, ZF1035855, ZF1056827, ZF1068325, ZF1068941, ZF1080034, ZF1102952, ZF1113498, ZF1114370, and ZF1125517. AD-24802lots ZF1025245, ZF1046888, ZF1057494, ZF1068892, ZF1080134, ZF1091014, ZF1091171, ZF1091593, ZF1102950, ZF1113494, ZF1114114, ZF1125215, and ZF2015711. AD-24854lots ZF1013537, ZF1024554, ZF1035413, ZF1036310, ZF1046999, ZF1047230, ZF1056918, ZF1057633, ZF1068902, ZF1079269, ZF1079743, ZF1091012, ZF1102545, ZF1103152, ZF1114358, ZF1125139, and ZF2015853. AD-24854-NLlots ZF1013534, ZF1013996, ZF1035415, ZF1036314, ZF1047232, ZF1056916, ZF1079745, ZF1080316, ZF1080521, and ZF1091239. AD-25703lots ZF1013933, ZF1025162, ZF1035869, ZF1036227, ZF1046576, ZF1047364, ZF1068539, ZF1079142, ZF1079563, ZF1102242, ZF1102935, ZF1103232, ZF1113477, ZF1113861, ZF1114337, ZF1114661, and ZF2016129. AD-25802-OBlots ZF1035537, ZF1057086, ZF1068592, ZF1080274, ZF1080835, ZF1091595, ZF1092074, ZF1102288, ZF1102572, ZF1102786, ZF1125007, and ZF2016072. AD-25855lots ZF1047288, ZF1057278, ZF1079689, and ZF1080527. AD-26702lots ZF1014152, ZF1035785, ZF1047324, ZF1057505, ZF1079822, ZF1102346, ZF1102553, ZF1113647, ZF2016688, and ZF2016989. AG-25854-Elots ZF1047326 and ZF1068572. ARCS-22122-F— — lot ZF1025264. ARCS-22123-Flots ZF1025266 and ZF1036280. ARCS-22703-Elots ZF1025247, ZF1036221, and ZF2016691. ARCS-22802lots ZF1025270 and ZF1057860. ARCS-22854-E— — lot ZF1035743. ARCS-22855lots ZF1035652, ZF1036225, ZF1057858, ZF1102654, ZF1102996, ZF1113529, ZF1114218, ZF1114550, ZF1125252, ZF2015917, and ZF2016589. - Amount recalled
- 634,912
Where it was sold
Why it was recalled
Stop using this product now
Lidstock of product does not contain chlorhexidine contraindication and contains wording "contains no medication" on the label. Product insert does reflect medicated status.
Using this product could cause serious injury, illness or death — stop using it now.
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