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Kentec Medical Inc

Kentec Medical Inc Recalls

All product recalls associated with Kentec Medical Inc.

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Recall Summary

Total Recalls

1000

Past Year

896

Class I (Serious)

125

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 15901–15920 of 17592 recalls

Kentec Medical Inc: Reusable Ohmeda Compatible Finger Clip Sensor, Model Numb...

Incompatible components: The Finger Clip Sensors - with a Serial Number prefix of PA514, PA515, YE508, ZC502 and ZG512 - are missing an additional diode and higher resistor in its existing configuration making them inoperable when used to interface with those Ohmeda Tuffsat monitors previously re-configured by Ohmeda to include a detection circuit for diodes.

FDAMay 18, 2007Nationwide• Kentec Medical Inc

GE OEC Medical Systems, Inc: Cleaning probe included as an accessory to aspirators tha...

Cleaning probes used to unclog disposable aspirators may shed small particles of nylon material which may be transferred into the nasal cavity.

FDAMay 18, 2007Nationwide• GE OEC Medical Systems, Inc

Becton Dickinson & Company: BD Microtainer Tube with Glycolytic Inhibitor, Catalog Nu...

Mislabeling : box and bag labels are incorrectly labeled to indicate the product contains Sodium Fluoride/Potassium Oxalate, however the instructions for use and the product itself are correct in the additive indicated and used (Sodium Fluoride/Na2EDTA).

1...794 795796797 798...880

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FDAMay 17, 2007Nationwide• Becton Dickinson & Company

Dishwashers (GE) – Fire Risk (2007)

Fire/Burn Risk

The recall includes GE built-in dishwashers sold under the following brand names: Eterna, GE, GE Profile™, GE Monogram®, Hotpoint®, and Sears-Kenmore. The dishwashers were sold in white, black, almond, bisque and stainless steel. The brand name is printed on the dishwasher's front control panel. The following model and serial numbers can be found inside the dishwasher tub on the front left side of the dishwasher. Brand Model Numbers Must Begin With Serial Numbers Must Begin With Eterna EDW20, EDW30 SS, TS, VS, ZS, AT, DT, FT, GT, HT, LT, MT, RT, ST, TT, VT, ZT, AV, DV, FV, GV, HV, LV, MV, RV, SV, TV, VV, ZV, AZ, DZ, FZ, GZ, HZ, LZ, MZ, RZ, SZ, TZ, VZ, ZZ, AA, DA, FA, GA, HA, LA, MA, RA, SA, TA, VA, ZA GE and GE Profile GHD50, GSD40, GSD41, GSD43, GSD46, GSD4910Z, GSD4920Z, GSD4930Z, GSD4940Z0, GSD50, GSD51, GSD521, GSD522, GSD523, GSD531, GSD532, GSD533, GSD535, GSD536, GSD55, GSD56, GSD57, GSD58, GSD59, GSDL3, GSDL6 GE Monogram ZBD3500Z0 Hotpoint HDA3400F, HDA35 SS, TS, VS, ZS, AT, DT, FT, GT, HT, LT, MT, RT, ST, TT, VT, ZT, AV, DV, FV, GV, HV, LV, MV, RV, SV, TV, VV, ZV, AZ, DZ, FZ, GZ, HZ, LZ, MZ, RZ, SZ, TZ, VZ, ZZ GE and GE Profile GHD35, GSD21, GSD2200D, GSD2200F, GSD2200G, GSD2201F, GSD2220F, GSD2221F, GSD2230F, GSD2231F, GSD2250F GSD23, GSD26, GSD27, GSD3115F, GSD3125F, GSD3135F, GSD3200G, GSD3210F, GSD3220F, GSD3230F, GSD33, GSD341, GSD342, GSD343, GSD345, GSD3610F, GSD3620F, GSD3630F, GSD3650F GSD37, GSD381, GSD382, GSD383, GSD385, GSD391, GSD392, GSD393, GSD4525F, GSD4535F, GSD4555F, GSDL122F, GSDL132F, GSDL24, GSM2100F, GSM2100G, GSM2100Z0, GSM2110D, GSM2110F, GSM2130D, GSM2130F Sears-Kenmore 363.1438, 363.1447, 363.1445, 363.1448, 363.1457, 363.1467, 363.1475, 363.15161792, 363.1517, 363.1521, 363.1527, 363.1528, 363.1531, 363.1532, 363.1546, 363.1547, 363.1548, 363.1556, 363.1565, 363.1567, 363.1617, 363.1655 SS, TS, VS, ZS, AT, DT, FT, GT, HT, LT, MT, RT, ST, TT, VT, ZT, AV, DV, FV, GV, HV, LV, MV, RV, SV, TV, VV, ZV, AZ, DZ, FZ, GZ, HZ, LZ, MZ, RZ, SZ, TZ, VZ, ZZ

CPSCMay 16, 2007Nationwide• GE Consumer & Industrial, of Louisville, Ky.

Smiths Medical PM, Inc.: Pneupac VR1 Standard and VR1 Responder is a hand held por...

Smiths Medical is conducting a recall of 93 Pneupac VR1 Emergency & Transport Ventilators following the identification of a problem which may exist with the demand valve that could cause the ventilator to stop cycling & to deliver continuous flow output to the patient.

FDAMay 16, 2007Nationwide• Smiths Medical PM, Inc.

Blackstone Medical, Inc.: Ascent POCTS (Posterior Occipital Cervical Thoracic Syste...

Manufacturing Defect: The saddle of the screw's body relative to the keyway exceeds the tolerance outlined in the device specifications. The extent to which the tolerance is exceeded varies from part to part, in the extreme the tolerance is exceeded by (+) 50%. As a consequence, there is a potential for set-screw cross-threading during implantation. Cross-threading could in turn lead to a comprom

FDAMay 15, 2007Nationwide• Blackstone Medical, Inc.

Heated Massage Recliners (Berkline) – Burn Hazard (2007)

Fire/Burn Risk

This recall involves the Berkline heated massage recliners with model number 13071 and piece code number 2700. The brand name, the model number, and the piece code can be found on the bill of sale and/or product packaging. The recliners were sold in brown and burgundy.

CPSCMay 11, 2007Nationwide• Berkline Benchcraft LLC, of Morristown, Tenn.

Embrace Infant Car Seat (Evenflo) – Fall Risk (2007)

The recall involves Evenflo Embrace™ Infant Car Seat/Carriers made before April 8, 2006. The recalled car seat/carriers have model numbers beginning with 317, 320, 397, 398, 540, 548, 549, 550, 556, 597, 598 or 599. The model number and production date information can be found on a white label on the bottom of the carrier and on the top of the convenience base. Models beginning with "5" are units sold with the travel system (compatible stroller). "Evenflo" is on the carrying handle and car seat base. Embrace™ infant car seat/carriers made on or after April 8, 2006 are not included in this recall.

CPSCMay 10, 2007Nationwide• Evenflo Company Inc., of Vandalia, Ohio

Beckman Coulter Inc: Cytomics FC 500 Flow Cytometry System with CXP Software V...

Incorrect Display: In certain modes, the protocol will not initially display the correct data in some plots. In addition, when running EWL files, any edited SampleID1 is not automatically updated in all tubes in the panel.

FDAMay 4, 2007Nationwide• Beckman Coulter Inc

Coast Spas (Coast Spas) – Fire Hazard (2007)

Fire/Burn Risk

The recalled spas were manufactured from January 2002 through October 2004. Only spas manufactured during this time frame with either red or yellow pump and motor assemblies are included in this recall. The spa manufacturer's name and date code and the pump and motor assembly can be located in the spa compartment as shown below. Consumers can access this compartment by lifting out the compartment door and setting it aside.

CPSCMay 3, 2007Nationwide• Coast Spas Manufacturing Inc., of Langley, British Columbia, Canada (spas)

Varian Medical Systems Inc: Varian Medical Systems Clinac Medical Linear Accelerator....

The wedge tray may slip out of the Clinac interface mount during gantry rotation.

FDAMay 2, 2007Nationwide• Varian Medical Systems Inc

Philips Medical Systems North America Co. Phillips: Achieva MRI

Potential for gaseous helium to improperly vent, resulting in rupture of the magnet vessel and venting of helium into the MRI site.

FDAApr 30, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Gyroscan MRI

Potential for gaseous helium to improperly vent, resulting in rupture of the magnet vessel and venting of helium into the MRI site.

FDAApr 30, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Intera MRI

Potential for gaseous helium to improperly vent, resulting in rupture of the magnet vessel and venting of helium into the MRI site.

FDAApr 30, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Panorama 1.0T MRI

Potential for gaseous helium to improperly vent, resulting in rupture of the magnet vessel and venting of helium into the MRI site.

FDAApr 30, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems (Cleveland) Inc: The product is an isolation transformer, an accessory to ...

Fire/Burn Risk

The TEAL Power Conditioning units may fail and result in the unit emitting fire and/or smoke. Note: the TEAL Power Conditioning Unit has the potential to fail when the scanner that is attached to the TEAL is powered and in use as well as when not in use.

FDAApr 27, 2007Nationwide• Philips Medical Systems (Cleveland) Inc

Medtronic MiniMed: Medtronic MiniMed Paradigm Insulin Infusion Pumps for the...

Exposure to Magnetic Resonance Imaging (MRI) has resulted in damage to the component that monitors and controls movement of the motor in the MiniMed Paradigm insulin infusion pump. Although there were alarms as a result of the damage, some users cleared these alarms and continued using the pump. Under such conditions, the pump will significantly over-deliver; potentially causing severe hypoglycemi

FDAApr 27, 2007PR• Medtronic MiniMed

Medtronic Emergency Response Systems, Inc.: LIFEPAK 20 defibrillator/monitor. The device is an AC pow...

White Screen Lock up: LifePak 20 defibrillators with software version 48 or version 52 may experience an intermittent timing issue during the power on sequence. This may lock up the device resulting in the monitor screen going white, and may cause a potential delay or prevention of shock treatment.

FDAApr 27, 2007IN, OR• Medtronic Emergency Response Systems, Inc.

Polaris Snowmobiles – Control Loss Risk (2007)

Only 2006 model year Polaris snowmobiles are part of this recall. The model and serial number identification decal is located on the right side of the tunnel underneath the seat. The recalled model names and numbers are listed below. Models Affected Model Numbers 2006 FS Classic S06PD7ES 2006 FST Classic S06PD7FS/S06PD7FE 2006 FS Touring S06PT7ES 2006 FST Touring S06PT7FS 2006 FST Switchback S06PS7FS/S06PS7FE

CPSCApr 26, 2007Nationwide• Polaris Industries Inc., of Medina, Minn.

Philips Medical Systems: HD11XE Diagnostic Ultrasound System

Potential for erroneous measurements which may lead to incorrect diagnosis based upon the presence of an inaccurate, undetectable error in clinical measurement or calculation. If the user exits an imaging mode while Active Annotation is in use, the system can enter an undefined state where the image scale calibration may not match the scale of the on-screen measurements and graphics and possib

FDAApr 25, 2007Nationwide• Philips Medical Systems