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    RNAgents Total RNA Isolation System (Cat. # Z5110). Kit Box label/Box drawer label. For Laboratory Use. Promega Corporation, Madison, WI. USA. Bottle Label: Phenol: Chloroform: Isoamyl Alcohol (Cat.# Z5112). Part Two of Two of Z5110. Size 100ml. For laboratory Use. A component of the RNAgents Total RNA Isolation System. The RNAgents Total RNA Isolation System provides a scalable method for RNA isolation from 6 grams of tissue or 6 x 10 (eighth power) cultured cells. The system reduces the level of chromosomal DNA, a major advantage when the downstream application of amplification and analysis of RNA transcripts is desired. Isolated RNA can be resuspended in any volume, making the system ideal for microarrays.

    FDA Recall
    Terminated ·Promega Corpopration·Product code LTD·June 4, 2008

    Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Ltd Tiger Large Cannulated Screw System, Model 215-00-001; and (2) Trilliant Surgical Ltd Large Cannulated Headless Screw System, Model 215-00-001. The firm name on the label is Trilliant Surgical Ltd., Houston, TX.

    FDA Recall
    Terminated ·Trilliant Surgical, LLC·Product code HWC·July 19, 2018

    Instructions for Use and Surgical Cleaning Sterilization Protocol for Trilliant Surgical Ltd Twist Sublatar Implant System, Model 112-00-001. The firm name on the label is Trilliant Surgical, Ltd, Houston, TX.

    FDA Recall
    Terminated ·Trilliant Surgical, LLC·Product code HWC·July 19, 2018

    Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Gridlock Plating System, Model 310-01-100. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.

    FDA Recall
    Terminated ·Trilliant Surgical, LLC·Product code HWC·July 19, 2018

    Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of 10- 100 ml vials. The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England and Oxoid Ltd., Basingstoke, Hants, England.

    FDA Recall
    Terminated ·Remel Inc·Product code JSK·February 5, 2015

    Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Gridlock Ankle Plating System, Model 320-01-100. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.

    FDA Recall
    Terminated ·Trilliant Surgical, LLC·Product code HWC·July 19, 2018

    Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Disco Subtalar Implant System, Model 112-00-001. The firm name on the label is Trilliant Surgical, Ltd, Houston, TX.

    FDA Recall
    Terminated ·Trilliant Surgical, LLC·Product code HWC·July 19, 2018

    Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Small Joint Reaming System, Model 311-00-001. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.

    FDA Recall
    Terminated ·Trilliant Surgical, LLC·Product code HWC·July 19, 2018

    Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd 3S Hemi Toe Implant System, Model 111-00-001. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.

    FDA Recall
    Terminated ·Trilliant Surgical, LLC·Product code HWC·July 19, 2018

    Instructions for Use and Surgical Cleaning and Sterilization Protocol for Trilliant Surgical Ltd Two-Step Hammertoe Implant System, Model 214-00-001. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.

    FDA Recall
    Terminated ·Trilliant Surgical, LLC·Product code HWC·July 19, 2018

    ENCORE (R) Microptic (R) Powder-Free Latex Surgical Gloves, 1 Pair, Size 5, Sterile R, CE 0086, EC REP Ansell (UK) Ltd., Tamworth, Staffordshire, B79 7UL UK, Ansell Lanka (pvt) Ltd., Biyagama Export Processing Zone, Biyagama, Sri Lanka Intended use: Surgical Gloves

    FDA Recall
    Terminated ·Ansell Healthcare Products LLC·Product code KGO·September 3, 2010

    Outback LTD Re-Entry Catheter, Sterile, Single Use. The Cordis LuMend OUTBACK LTD Re-Entry Catheter is indicated for placement and positioning of guidewires within the peripheral vasculature. The cannula is a nitinol needle that is used to re-enter the true lumen of the vessel.

    FDA Recall
    Terminated ·Cordis Corporation·Product code MCW·August 20, 2008

    Medpro AccuFlo Elastomeric Infusion Device, Model #CT-0020-270C, packaged 12/box. The box label shows the product is Manufactured By: Medpro International (Thailand) Ltd. for Medpro Corporation Pte. Ltd., Singapore. The devices are intended for patients requiring intravenous, percutaneous, subcutaneous, intra-operative sites or epidural administration of medications.

    FDA Recall
    Terminated ·Progressive Medical Inc·Product code MEB·July 28, 2011

    King LT-D Oropharyngeal Airways The King LT-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents.

    FDA Recall
    Terminated ·King Systems Corp.·Product code CAE·September 3, 2013

    Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Ltd Tiger Headless Cannulated Screw System, Model 212-00-001; and (2) Combination Tiger Cannulated/Tiger Headless Cannulated Screw System, Model 210-00-101. The firm name on the label is Trilliant Surgical Ltd, Houston, TX.

    FDA Recall
    Terminated ·Trilliant Surgical, LLC·Product code HWC·July 19, 2018

    Gelweave (TM) Vascular Prostheses Manufactured by - VASCUTEK Ltd a TERUMO company

    FDA Recall
    Terminated ·Vascutek, Ltd. Newmains Avenue Inchinnan United Kingdom·Product code DSY·July 15, 2014

    TM-300 Traction System; an Rx software driven device used for patient traction; Manufactured for Sammons Preston Roylan, An Ability One Company, Bolingbrook, IL 60440, Manufactured by: ITO Co., Ltd., 3-3-3 Toyotama-Minami, Nerima-ku, Tokyo, 176-8605, Japan

    FDA Recall
    Terminated ·Sammons Preston Rolyan, An Ability One Company·Product code HST·July 13, 2005

    EpiFix Fixation Device for Epidural Catheters, REF 670M, Unomedical, Ltd., Great Britain.

    FDA Recall
    Terminated ·Merit Medical Systems, Inc·Product code KMK·February 15, 2007

    Neutralect Diathermy Cable, Unomedical Ltd., Ref code 3508M, and Ref Code 3405M.

    FDA Recall
    Terminated ·ConvaTec·Product code GEI·January 22, 2010

    Sonopet Ultrasonic Surgical System, Model UST-2001, Manufacturer Miwatec Co. LTD, Tokyo, Japan.

    FDA Recall
    Terminated ·Stryker Instruments Div. of Stryker Corporation·Product code LFL·July 15, 2010