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Crédits
Manufacturers
Smiths Medical ASD, Inc.
Adresse du fabricant
Smiths Medical ASD, Inc., 10 Bowman Dr, Keene NH 03431-5043
Société-mère du fabricant (2017)
Smiths Group Plc
Source
USFDA
168 Events
Rappel de Device Recall Smiths Medical
Rappel de Device Recall Smiths Medical
Rappel de Device Recall Smiths Medical
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Rappel de Device Recall Portex Anaerobic Pulsator Arterial Blood Sampling Kit
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Rappel de Portex Per-Fit Percutaneous Dilational Tracheostomy Kit ,ID 7.0mm || Product Number: || 535070
Rappel de Portex Per-Fit Percutaneous Dilational Tracheostomy Kit, ID 8.0mm || Product Number: 535080
Rappel de Portex Per-Fit Percutaneous Dilational Tracheostomy Kit , ID 9.0mm || Product Number: 535090
Rappel de Portex Per-Fit Percutaneous Dilational Tracheostomy Kit , ID 7.0mm || Product Number: 538070E
Rappel de Portex Per-Fit Percutaneous Dilational Tracheostomy Kit , ID 8.0mm || Product Number: 538080E
Rappel de Portex Per-Fit Percutaneous Dilational Tracheostomy Kit , ID 9.0mm || Product Number: 538090E
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Rappel de Spinal Anesthesia Trays
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Rappel de Low Dead Space Connector with Sideport, 3.5mm
Rappel de Portex
Rappel de Device Recall Wallace SurePro/ SurePro Ultra Embryo Replacement Catheters
Rappel de Device Recall Wallace SurePro Ultra Embryo Replacement Catheter with Obturator
Rappel de Device Recall Wallace SurePro Ultra Embryo Replacement Catheter with Stylet
Rappel de Device Recall Wallace SurePro Two Stage Embryo Replacement Catheter with Obturator
Rappel de Device Recall Wallace SurePro Two Stage Embryo Replacement Catheter for difficult transfer with Stylet
Rappel de Device Recall Wallace SurePro Single Stage Embryo Replacement Catheter
Rappel de Device Recall Portex Arterial Blood Sampling Line Draw Syringes
Rappel de Device Recall Portex Arterial Blood Sampling Line Draw Syringes
Rappel de Device Recall Portex Arterial Blood Sampling Line Draw Syringes
Rappel de Device Recall Portex Arterial Blood Sampling Line Draw Syringes
Rappel de Device Recall Portex Arterial Blood Sampling Line Draw Syringes
Rappel de Device Recall Portex Arterial Blood Sampling Line Draw Syringes
Rappel de Device Recall Portex Arterial Blood Sampling Line Draw Syringes
Rappel de Device Recall Portex Arterial Blood Sampling Line Draw Syringes
Rappel de Device Recall Portex Arterial Blood Sampling Line Draw Syringes
Rappel de Device Recall Portex Arterial Blood Sampling Line Draw Syringes
Rappel de Device Recall Portex Arterial Blood Sampling Line Draw Syringes
Rappel de Device Recall Portex Arterial Blood Sampling Line Draw Syringes
Rappel de Device Recall Portex Arterial Blood Sampling Line Draw Syringes
Rappel de Device Recall Smiths Medical
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Rappel de Device Recall Portex Endotracheal Tube Holders
Rappel de Device Recall Portex Endotracheal Tube Holders
Rappel de Device Recall Portex Endotracheal Tube Holders
Rappel de Device Recall Portex Endotracheal Tube Holders
Rappel de Device Recall Portex Endotracheal Tube Holders
Rappel de Device Recall Portex Endotracheal Tube Holders
Rappel de Device Recall Portex Continuous Epidural Tray
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163 dispositifs dans la base de données
Device Recall Smiths Medical
Modèle / numéro de série
Lot Numbers: 2756526, 2771498
Classification du dispositif
General Hospital and Personal Use Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
US Nationwide Distribution in the states of AZ CA FL GA IL IN LA MA MN MO MS MT NC ND NJ NV NY OH OR PA RI TN TX VA WA WI WV
Description du dispositif
Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 10mL Luer lock syringe; Reorder Number: 4102010 || Product Usage: || The Needle Pro¿ Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.
Device Recall Smiths Medical
Modèle / numéro de série
Lot Number: 2755713
Classification du dispositif
General Hospital and Personal Use Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
US Nationwide Distribution in the states of AZ CA FL GA IL IN LA MA MN MO MS MT NC ND NJ NV NY OH OR PA RI TN TX VA WA WI WV
Description du dispositif
Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 5mL Luer lock syringe; Reorder Number: 452010 || Product Usage: || The Needle Pro¿ Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.
Device Recall Smiths Medical
Modèle / numéro de série
Lot Numbers: 2731779, 2763138, 2771516, 2771517
Classification du dispositif
General Hospital and Personal Use Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
US Nationwide Distribution in the states of AZ CA FL GA IL IN LA MA MN MO MS MT NC ND NJ NV NY OH OR PA RI TN TX VA WA WI WV
Description du dispositif
Hypodermic Needle Pro¿ Edge" Safety Device 20G x1; Reorder Number: 402010 || Product Usage: || The Needle Pro¿ Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.
Device Recall Portex
Modèle / numéro de série
Lot Number: K516574
Classification du dispositif
Anesthesiology Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide
Description du dispositif
15816-21 SPINAL(DD) 27G QUINCKE W/DRUGS
Device Recall Portex
Modèle / numéro de série
Lot Number: K516550
Classification du dispositif
Anesthesiology Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide
Description du dispositif
15830-21 SPINAL(DD) 25G WHITACRE W/DRUGS
158 en plus
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En savoir plus sur les données
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Smiths Medical Asd, Inc.
Société-mère du fabricant (2017)
Smiths Group Plc
Source
NIDFSINVIMA
Smiths Medical ASD, Inc.
Adresse du fabricant
Smiths Medical ASD, Inc., 1265 Grey Fox Rd, Saint Paul MN 55112-6929
Société-mère du fabricant (2017)
Smiths Group Plc
Source
USFDA
Smiths Medical ASD, Inc.
Adresse du fabricant
Smiths Medical ASD, Inc., 5700 W 23rd Ave, Gary IN 46406-2617
Société-mère du fabricant (2017)
Smiths Group Plc
Source
USFDA
Smiths Medical ASD, Inc.
Adresse du fabricant
Smiths Medical ASD, Inc., 160 Weymouth St, Rockland MA 02370-1136
Source
USFDA
Smiths Medical ASD, Inc.
Société-mère du fabricant (2017)
Smiths Group Plc
Source
MHSIDCCCDMIS
8 en plus
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