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Notices in alphabetical order
by manufacturer
(2006 - 2010)

A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z

Note: To find recall articles from the past 12 months, log in to Supply Chain Advisor. Click on the News-Resources tab (Select "recalls" under content type and then search by specific product, contract category and/or date range). Consult the FDA Web site and/or the manufacturer for additional information. Listing of notices in chronological order of date issued.

A

Abbott

Alcon Research LTD

Alliant Healthcare

AngioScore Inc.

  • AngioScore Inc., AngioSculpt Percutaneous Transluminal Angioplasty (PTA) Scoring Balloon CatheterOTW 0.018" Platform (multiple sizes) 01/05/11

Ansel Healthcare

Apogee Medical

Arrow

  • Arrow International, Inc. issues recall on TransRadial Artery Access Products (10/28/2013)
  • Arrow International announces recall on Central Venous Catheter Kit (7/25/2013)
  • Arrow Ultra 8 Intra-Aortic Balloon Catheters (IABS) 8 FR 30CC and 40CC Universal and Arrow Intra-Aortic Balloon (IAB) Catheter with a Fiber Optic Sensor and Measurement System: UPDATE 01/26/2011 01/26/11

Arstasis

  • Arstasis One Access System 02/09/11

Arizant

Ascent

Atrium Medical Corporation

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B

Bard

Baxa

Baxter

  • Baxter Healthcare Corporation issues recall on Potassium Chloride Injection 6/29/2011
  • Baxter issues urgent device correction on AUTOMIX compounder 2/16/2011
  • Baxter Colleague Single and Triple Channel Volumetric Infusion Pumps - Recall, Refund and Replacement 11/30/10

Bayer Healthcare

 

Beckton Dickinson (BD)

Beckman Coulter

Becton, Dickson and Company

Boston Scientific

B. Braun Medical

  • B. Braun addEASE Binary Connector 11/30/10
  • B. Braun, Outlook 400ES Safety Infusion System, Model Number 621-400ES 01/31/11

Biomerieux

Braco

 

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C

CareFusion

  • CareFusion issues medical device recall for needlefree connector (1/24/2014)
  • CareFusion voluntary recall of PVP-I Scrub Brushes (1/3/2014)
  • CareFusion issues medical device recall for Alaris PC unit (12/10/2013)
  • Carefusion issues urgent product recall. Carefusion released a customer letter regarding potential risk associated with AVEA® ventilators when used at higher altitudes. (9/10/2013)
  • CareFusion issues recall/notice on Alaris PC Unit (model 8015) (8/2/2012)
  • URGENT RECALL NOTICE: CareFusion AirLife Infant Breathing Circuit
  • CareFusion 211 Inc. issues recall/notice on AVEA® ventilator, all models 10/11/11
  • CareFusion Corporation, Alaris PC Units (Model 8015) 10/15/10

Cardinal

Cepheid

Cobe Cardiovascular

ConMed

Cook

Country Pure Foods, Inc.

Covidien

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D

Davol Inc.

DeRoyal

Draeger Medical, Inc.

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E

Edwards Lifesciences Corp.

Ethicon

EV3

  • ev3 NanoCross .014" OTW PTA Dilatation Catheter 12/28/10

Excelsior

  • Excelsior Medical Disposable Syringe with Normal Saline (0.9% Sodium Chloride, 5mL fill in 6mL syringe) 10/26/10

 

 

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F

Fresenius

  • Fresenius Medical Care North America, CombiSet True Flow Series Hemodialysis Blood Tubing Set with Priming Set and Transducer Protectors for Use with the Blood Volume Monitor 01/20/11
  • Fresenius Kabi LLC, Red Blood Cell (RBC) Exchange Sets used on AS104 Blood Cell Separation Devices 12/21/10

FDA

G

Gaymar

GE

Gore, W. L.

Guidant

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H

Hettich

Hospira

  • Hospira issues urgent drug recall on one lot of Aminosyn II 10 percent (9/21/2013)
  • Hospira issues urgent medical device field correction letter (9/17/2013)
  • Hospira issues urgent drug recall on one lot of Dobutamine in 5% Dextrose Injection (5/6/2013)
  • Hospira issues urgent device field correction for Lifecare PCA (3/21/2013)
  • Hospira issues important device information for Lifecare PCA (3/21/2013)
  • Hospira issues urgent device field correction for Lifecare PCA (3/21/2013)
  • Hospira issues market withdrawal on 0.9% Sodium Chloride injection, USP, 1000 mL (3/21/2013)
  • Hospira issues information regarding importation of infusion devices (3/21/2013)
  • Hospira issues urgent device field correction letter (3/21/2013)
  • Hospira issues urgent device recall (3/13/2013)
  • Hospira issues recall on 0.9% Sodium Chloride, USP, 50 mL (3/13/2013)
  • Hospira announced that it is initiating a voluntary recall on one lot of 0.9% Sodium Chloride, USP, 50 mL, lot number 22-028-JT (2/27/2013)
  • Hospira announced that it is initiating an urgent device recall for minibore extension set, 59 inch with spin lock collar, non-DEHP, latex-free (2/27/2013)
  • Hospira Worldwide announces IV supply interruption on large volume solutions (1/30/2013)
  • Hospira issues voluntary nationwide recall of one lot of lactated ringers and 5% dextrose injection, USP, 1000 mL, flexible containers due to mold contamination (10/31/2012)
  • Hospira Inc. issues recall on specific lot of 0.9% Sodium Chloride Irrigation, USP, 3000 mL, Flexible Container  3/7/2013
  • Hospira Inc. is voluntarily recalling one lot of list number 7922-02 5% Dextrose Injection 9/14/2011
  • Hospira issues nationwide recall alert on 0.9% Sodium Chloride Injection USP in 1000 mL Lot # 95-070-JT 3/30/11
  • Hospira Symbiq One and Two Channel Infuser 11/04/10

I

Integra NeuroSciences

Ikaria Holdings

J

Johnson & Johnson

K

Kimberly Clark

L

LANX

Lantheus Medical Imaging

Leonhard Lang

Liko

Lumenis

M

Madela, Inc.

Mallinckrodt

Maquet, Inc. (a division of Getinge, Inc.)

Medivators

Medline Industries

Medtronic

  • Medtronic, Inc. issues recall on Interventional Wires and Attain Hybrid Guidewires (11/20/2013)
  • Medtronic Octopus Nuvo Tissue Stabilizer, Model TSMICS1 11/02/10

Merit

  • Merit Medical Systems Prelude Short Sheath Catheter Introducer 02/04/11

Metrex Research

Micromedics Inc.

  • Micromedics, Inc., Surgical Sealant Dispensers, Micromedics Nasal Septal Buttons, and Otological Ventilation Tubes - Sealed in Pouches 11/23/10

Moog Medical Devices

  • Moog Medical Devices Group Issues Urgent Medical Device Recall 3/29/11

Multi-Med

  • Multi-Med, Inc. Huber (Non-coring) Needles and Finished Devices Containing Huber Needles Labeled as "All-Med Medical Products, Inc." and "Marquette Medical, Inc." Brands and Provided to Some Consignees in Bulk Without Labeling 10/12/10

 

N

Natus

O

Olympus America

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P

Posey

Penumbra

  • Penumbra System Reperfusion Catheter 032 12/08/10

Physio-Control Inc.

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R

Respironics

S

Sage Products, Inc.

Siemens

  • Siemens Healthcare Diagnostics issues recall on B12 Flex Reagent Cartridge (K6442) 5/16/2012
  • Shelhigh

    Sigma

    • Sigma issues recall on Spectrum Infusion Pump Model 35700 7/18/2011
    • SIGMA Spectrum Infusion Pump Model 3570 11/12/10

    Smith & Nephew, Inc.

    Smiths Medical

    Spacelabs Medical

    STERIS

    St. Jude Medical

    Stryker

    Symbig

    T

    Talecris

    Teleflex Medical

    Triad

    • Triad Group, Triad Sterile Lubricating Jelly 02/15/11

    Tri-anim

    Terumo

    U

    Utah Medical

    V

    Vanguard

    W

    WalkMed

    • WalkMed, Inc. Triton Pole Mount Infusion Pump 11/24/10

    Westmed Inc.

    • Westmed Inc., BagEasy Manual Resuscitation Devices 10/13/10

    Z

    Zimmer Orthopaedic

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