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TTI Floor Care North America, of Glenwillow, Ohio

TTI Floor Care North America, of Glenwillow, Ohio Recalls

All product recalls associated with TTI Floor Care North America, of Glenwillow, Ohio.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

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 17841–17860 of 21320 recalls

Dirt Devil Power Brush Attachment – Laceration Risk (2008)

Laceration Risk

The recalled Dirt Devil Turbo Tool/Power Brush attachment was sold as an accessory with the following Dirt Devil vacuum models. Only vacuum tool accessories with date codes J7060 through J7365 and have a C-clip connector are included in this recall. The date code is located on the underside of the vacuum accessory. The Turbo Tool/Power Brush tools are about 6 ½ inches long by about 5 inches wide and come in a variety of colors that match the color of the vacuum. The housing of the tool was made in clear, red, green, or light blue with clear, light blue, dark blue, red, purple, or black turbine fans with matching brush rolls. Dirt Devil Vacuum Models Reaction Purpose for Pets Ultra Swivel Glide M110000 M140000 M086020 M110000HD M140000CA M110001B M110002 Envision Wide Glide Swerve M110003 M086700WCA M086030 M110006 M086710 M086030CA M110008 M110008CA Action Upright Royal Commercial M110009 M110020CAB RY6100

CPSCJul 23, 2008Nationwide• TTI Floor Care North America, of Glenwillow, Ohio

Siemens Medical Solutions, USA, Inc: Siemens KinetDx 4.2 Workplace, Siemens Medical Solutions,...

If the text is manually modified and additional phrases added as a result of worksheet interactions, some of the phrases may not populate the report.

FDAJul 23, 2008Nationwide

1...891 892893894 895...1066

Page 893 of 1066Next

• Siemens Medical Solutions, USA, Inc

Philips Medical Systems: Philips Telemonitoring System Software (M3811B) used with...

Software: If Weight Limits edited, values will return to default values that were deleted

FDAJul 22, 2008Nationwide• Philips Medical Systems

BD Diagnostics (GeneOhm Sciences, Inc): BD GeneOhm MRSA 200 ct, Catalog #441242. IDI-MRSA assay...

BD Diagnostics GeneOhm (BDDG) initiated the recall after they identified that the product has the potential to identify a patient as falsely positive for colonization with methicillin resistant Staphylococcus aureus. The potential health hazard related to a false positive result from this assay would be that a patient may be misclassified as having MRSA colonization when in fact they do not have

FDAJul 21, 2008Nationwide• BD Diagnostics (GeneOhm Sciences, Inc)

Siemens Medical Solutions Diagnostics: IMMULITE/IMMULITE 1000 Progesterone (LKPG 1,5) For in vi...

Siemens Healthcare Diagnostics has confirmed a long-standing high bias with LKPG 1, 5. (The bias is approximately 25% at 10 - 20 ng/mL as opposed to approximately 3% at 1-3 ng/mL - for more detail see the bias plot that is included with this notice.).

FDAJul 21, 2008PR• Siemens Medical Solutions Diagnostics

BD Diagnostics (GeneOhm Sciences, Inc): BD GeneOhm MRSA 48 ct, Catalog #441244. IDI-MRSA assay i...

FDAJul 21, 2008Nationwide• BD Diagnostics (GeneOhm Sciences, Inc)

Synaptic Corp: Synaptic 3600 and 3800 with Cranial Electrical Stimulatio...

Device was distributed without marketing approval.

FDAJul 18, 2008Nationwide• Synaptic Corp

Apogee Medical, Inc: Apogee Intermittent Catheter, 10 Fr 15", Catalog/Ref No. ...

Laceration Risk

Due to a package seal defect the catheter tip may have been inadvertently cut which could cause trauma to the urethra upon use. Also the sterility of the product could be compromised.

FDAJul 17, 2008Nationwide• Apogee Medical, Inc

American Medical Systems: AMS 700 CX MS Pump IZ, Preconnect Penoscrotal, 18 cm, Ste...

The carton labeling does not match the product packaged inside. The package indicated that the device is an 18cm Preconnected MS pump while it is actually an 18cm Ultrex Preconnected MS Pump.

FDAJul 17, 2008LA• American Medical Systems

Apogee Medical, Inc: Apogee Intermittent Catheter with Coude tip, 12 Fr 16", C...

Laceration Risk

Due to a package seal defect the catheter tip may have been inadvertently cut which could cause trauma to the urethra upon use. Also the sterility of the product could be compromised.

FDAJul 17, 2008Nationwide• Apogee Medical, Inc

Apogee Medical, Inc: Apogee Intermittent Catheter, 6 Fr 15", Catalog/Ref No. 1...

Laceration Risk

Due to a package seal defect the catheter tip may have been inadvertently cut which could cause trauma to the urethra upon use. Also the sterility of the product could be compromised.

FDAJul 17, 2008Nationwide• Apogee Medical, Inc

SpeeCo Log Splitter Engines – Fire Hazard (2008)

Fire/Burn Risk

The recall involves Honda engines (model type GCV160LA N1A) used in Split Master by SpeeCo and Huskee brand log splitters. Only engine serial numbers between 5547012 and 6880908 are included in the recall. The serial number is located below the upper shroud near the oil dipstick. The following models of log splitters are affected by the recall and are either silver/black or red/black colored. Huskee Log Splitter LS401227TS (22 Ton) LS401228NO (27 Ton) SpeeCo Split Masters LS401228SP (22 Ton) LS401227NO (22 Ton) LS401225NO (25 Ton)

CPSCJul 17, 2008Nationwide• American Honda Motor Corp., of Torrance, Calif.

Honda TRX420 Rancher ATVs – Control Loss Risk (2008)

This recall involves Model Year 2007-08 Honda TRX420 ATVs, also known as the Honda FourTrax Rancher 4X4. These are adult-size ATVs designed for use by riders age 16 and older. The recalled ATVs are available in red, black, olive, and camouflage. The Honda name and wing logo are printed on the fuel tank. The model year is printed on a label located on the frame behind the left front wheel. The model name "Rancher" is on a label at the left rear of the ATV.

CPSCJul 17, 2008Nationwide• American Honda Motor Co. Inc., of Torrance, Calif.

Apogee Medical, Inc: Apogee Intermittent Catheter, 8 Fr 16", Catalog/Ref No. 1...

Laceration Risk

Due to a package seal defect the catheter tip may have been inadvertently cut which could cause trauma to the urethra upon use. Also the sterility of the product could be compromised.

FDAJul 17, 2008Nationwide• Apogee Medical, Inc

Medical Device Technologies, Inc.: Angiotech, Bone Marrow Harvest Needle, Medical Device Tec...

Product packaging for Bone Biopsy trays/blisters may have a hole in the formed tray.

FDAJul 16, 2008Nationwide• Medical Device Technologies, Inc.

Medical Device Technologies, Inc.: Angiotech, Bone Marrow Aspiration Needle, Medical Device ...

Product packaging for Bone Biopsy trays/blisters may have a hole in the formed tray.

FDAJul 16, 2008Nationwide• Medical Device Technologies, Inc.

Medical Device Technologies, Inc.: Angiotech, T-Lok Bone Marrow Biopsy Needle, Medical Devic...

Product packaging for Bone Biopsy trays/blisters may have a hole in the formed tray.

FDAJul 16, 2008Nationwide• Medical Device Technologies, Inc.

Medical Device Technologies, Inc.: Angiotech, Bone Marrow Biopsy Needle, Medical Device Tech...

Product packaging for Bone Biopsy trays/blisters may have a hole in the formed tray.

FDAJul 16, 2008Nationwide• Medical Device Technologies, Inc.

SRI Surgical: Various SRI Surgical Disposable Accessory Packs. SRI's...

Distribution of a product that did not meet specifications. (labeling error)

Class IIModerate

FDAJul 16, 2008Nationwide• SRI Surgical

SRI Surgical: Various SRI Surgical Disposable Accessory Packs. SRI's D...

Distribution of a product that did not meet specifications. (labeling error)

FDAJul 16, 2008Nationwide• SRI Surgical