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Crédits
Devices
Arrow
Modèle / numéro de série
Product No. AP-06015. Lot Number: 11953, 12024, 12048, MF2122834, MF2122873, MF3013094,MF3023399, MF3033565, MF3033661, MF3043929,MF3044026, MF3044155, MF3054297, MF3054407, MF3064741, MF3074954, MF3085360, MF3106021,MF4016605, MF4020460, MF4031011, MF4031501, MF4041930, MF4062927,MF4063051, MF4073944, MF4094579, MF4094883, MF4095027, MF4116113,MF4126523, MF5017401, MF5049107, MF5049320, MF5059727, MF5060170,MF5060348, MF5060463, MF5081716, MF5082118, MF5082247, MF5113788,MF5113989, MF5124143, MF6014773, MF6025691, MF6036470, MF6036928,MF6047447, MF6057759, MF6058188, MF6068647, MF6079327, MS3110160,MS4073806.
Classification du dispositif
General Hospital and Personal Use Devices
Classe de dispositif
2
Dispositif implanté ?
Yes
Distribution
Nationwide. The firm is NOT recalling from international accounts.
Description du dispositif
Implantable Vascular Access System -- Infusion Ports with Silicone Rubber Catheter. || Latex-free A Port. 10 Fr. Introducer Kit. || Ref. Product No. AP-06015
Manufacturer
Arrow International Inc
1 Event
Rappel de Arrow
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Fabricant
Arrow International Inc
Adresse du fabricant
Arrow International Inc, 2400 Bernville Rd, Reading PA 19605-9607
Société-mère du fabricant (2017)
Teleflex Incorporated
Source
USFDA
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ARGON Bone Marrow I-type aspirate/biopsy needles & ARGON Trap-Lok Bone Marrow biopsy needles
Modèle / numéro de série
ARGON Bone Marrow I-type aspirate/biopsy needles & ARGON Trap-Lok Bone Marrow biopsy needlesProduct codes: BMHN1304VX, DBMNI1501, DBMNI1601, DBMNJ0804TL, DBMNJ1104TL, DBMNI1601Lot Numbers: 11095380, 11095842, 11098707, 11089370, 11096115, 11088295, 11094182, 11088597, 11090527ARTG Number: 223222
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Modèle / numéro de série
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Manufacturer
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Super Arrow-Flex Percutaneous Sheath Introducer Set
Modèle / numéro de série
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Manufacturer
Teleflex Medical Australia Pty Ltd
ARROW Intra-Aortic Balloon Catheter and Percutaneous Insertion Kits
Modèle / numéro de série
ARROW Intra-Aortic Balloon Catheter and Percutaneous Insertion KitsProduct Codes : IAB-05830-LWS, IAB-05830-U, IAB-05840-LWS, IAB-05840-U, IAB-06830-U, IAB-06840-U and IAK-06845Multiple Batch Numbers affectedARTG Numbers: 101617, 106866 and 107249
Classification du dispositif
Cardiovascular Devices
Manufacturer
Teleflex Medical Australia Pty Ltd
Various Kits containing Anticoagulant Citrate Dextrose Solution, Solution A (ACDA) 30mL Vials (Su...
Modèle / numéro de série
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Manufacturer
Zimmer Pty Ltd
565 en plus
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