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Medical Device Technologies, Inc.

Medical Device Technologies, Inc. Recalls

All product recalls associated with Medical Device Technologies, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

34

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 17101–17120 of 21320 recalls

Medical Device Technologies, Inc.: Angiotech Galactography Kit. Galactography Kit 30ga with...

Medical Device Technologies doing business as Angiotech has conducted a recall on Angiotech Breast Localization Needles, Soft Tissue Biopsy Needles, Vascular Access Needles, Bone Biopsy Needles, Access Needles, Galactography Kit, Stabilization Needles and Needle Guides for packaging integrity.

FDASep 1, 2009Nationwide• Medical Device Technologies, Inc.

Stryker Howmedica Osteonics Corp.: Secur-Fit MAX Secure-FIT Plus Max Surgical Protocol. Sur...

Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone.

FDAAug 31, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Accolade System Surgical Technique; Accolade C - Cemented...

Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone.

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FDAAug 31, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: OnmiFit HFx Surgical Protocol 127 degree and 132 degree ...

Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone.

FDAAug 31, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Siemens Healthcare Diagnostics, Inc.: Dimension Vista System CHEM 1 CAL, Catalog Number KC110, ...

Siemens Healthcare Diagnostics, Inc. has confirmed high accuracy shifts with Dimension Vista URCA Flex reagent cartridge (various lots) when calibrating with some vials from CHEM 1 calibrator lot 9DM001.

FDAAug 31, 2009Nationwide• Siemens Healthcare Diagnostics, Inc.

Stryker Howmedica Osteonics Corp.: OmniFit Eon 127 degree and 132 degree Surgical Protocol; ...

Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone.

FDAAug 31, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: CuttingEdge Total Hip Instrumentation Surgical Protocol; ...

Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone.

FDAAug 31, 2009Nationwide• Stryker Howmedica Osteonics Corp.

ZOLL Medical Corporation, World Wide Headquarters: ZOLL R Series Defibrillator/Pacemaker/Monitor Used by qu...

Failure of Device to display ECG could delay delivery of defibrillation or pacing therapy.

FDAAug 31, 2009Nationwide• ZOLL Medical Corporation, World Wide Headquarters

Siemens Medical Solutions USA, Inc.: V5M TEE Transducer, when used with an ACUSON S2000 ultras...

If the transducer is not disconnected from the system after an automatic shutdown due to thermal limits being exceeded, then the next time it is used, the thermal safety guards do not take effect. Normally, the thermal limit before automatic image freeze (and therefore power shut off) occurs at 43 degrees Centigrade.

FDAAug 28, 2009Nationwide• Siemens Medical Solutions USA, Inc.

Unimed Surgical Products, Inc.: Extended PTFE Coated Blade electrosurgical electrodes, 6....

Unimed Surgical Products, Inc., Largo, FL initiated a voluntary recall of the Extended PTFE Coated Blade electrosurgical electrodes, product number ES0014, due to concerns regarding product sterility for Lot #042209-03.

FDAAug 28, 2009Nationwide• Unimed Surgical Products, Inc.

Medtronic Neuromodulation: Medtronic Indura 1P Intrathecal Catheter, model 8709SC, M...

Current labeling for Medtronic Sutureless Connector (SC) catheters and revision kits (hereafter referred to as SC catheters) incorrectly states that SC catheters are compatible with Medtronic IsoMed constant-flow infusion pumps. SC catheters are compatible with Medtronic SynchroMed II and SynchroMed EL pumps. Medtronic has determined that SC catheters are not compatible with IsoMed pumps.

FDAAug 27, 2009WA, PR• Medtronic Neuromodulation

Medtronic Neuromodulation: Medtronic Intrathecal Catheter, model 8731SC, Method of S...

Current labeling for Medtronic Sutureless Connector (SC) catheters and revision kits (hereafter referred to as SC catheters) incorrectly states that SC catheters are compatible with Medtronic IsoMed constant-flow infusion pumps. SC catheters are compatible with Medtronic SynchroMed II and SynchroMed EL pumps. Medtronic has determined that SC catheters are not compatible with IsoMed pumps.

FDAAug 27, 2009WA, PR• Medtronic Neuromodulation

Medtronic Neuromodulation: Medtronic Sutureless Pump Connector Revision Kit, model 8...

Current labeling for Medtronic Sutureless Connector (SC) catheters and revision kits (hereafter referred to as SC catheters) incorrectly states that SC catheters are compatible with Medtronic IsoMed constant-flow infusion pumps. SC catheters are compatible with Medtronic SynchroMed II and SynchroMed EL pumps. Medtronic has determined that SC catheters are not compatible with IsoMed pumps.

FDAAug 27, 2009WA, PR• Medtronic Neuromodulation

Medtronic Neuromodulation: Medtronic Intrathecal Catheter Pump Segment Revision Kit,...

Current labeling for Medtronic Sutureless Connector (SC) catheters and revision kits (hereafter referred to as SC catheters) incorrectly states that SC catheters are compatible with Medtronic IsoMed constant-flow infusion pumps. SC catheters are compatible with Medtronic SynchroMed II and SynchroMed EL pumps. Medtronic has determined that SC catheters are not compatible with IsoMed pumps.

FDAAug 27, 2009WA, PR• Medtronic Neuromodulation

Window Blinds (Vertical Land) – Strangulation Risk (2009)

This recall involves all Vertical Land custom-made vertical and cellular window coverings that do not have a cord tensioning device and horizontal blinds that do not have inner cord stop devices. A sticker identification label can be found on the head rail of some of the window coverings which lists the company's name, address and telephone number.

CPSCAug 26, 2009Nationwide• Vertical Land Inc., of Panama City Beach, Fla.

Boston Scientific Corporation: Boston Scientific Renegade" Hi-Flo Microcatheter, Periph...

Boston Scientific has determined that the sterile barrier in the packaging of the affected product may be compromised. It has been reported that the pouch seal (top seal) may be breached.

FDAAug 26, 2009GA, NM, WY +1 more• Boston Scientific Corporation

Boston Scientific Corporation: Boston Scientific Renegade" Hi Flo Microcatheter (neurov...

Boston Scientific has determined that the sterile barrier in the packaging of the affected product may be compromised. It has been reported that the pouch seal (top seal) may be breached.

FDAAug 26, 2009GA, NM, WY +1 more• Boston Scientific Corporation

Boston Scientific Corporation: Boston Scientific, Renegade Fiber Braided Microcatheter, ...

Boston Scientific has determined that the sterile barrier in the packaging of the affected product may be compromised. It has been reported that the pouch seal (top seal) may be breached.

FDAAug 26, 2009GA, NM, WY +1 more• Boston Scientific Corporation

Draeger Medical, Inc.: Drager Surgical Lights Sola 500 and Sola 700.

welded seam may fail

FDAAug 26, 2009Nationwide• Draeger Medical, Inc.

Smiths Medical Hythe Hythe, Kent United Kingdom: Portex Tracheal Tube, Cut to Length, Oral, Siliconized, 2...

Pediatric Trachel Tube manufactured with internal diameter smaller than indicated in the label may result in inability to remove secretions and cause partial or complete obstruction of the airway

FDAAug 25, 2009Nationwide• Smiths Medical Hythe Hythe, Kent United Kingdom