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North Coast Medi-Tek Inc

North Coast Medi-Tek Inc Recalls

All product recalls associated with North Coast Medi-Tek Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 23941–23960 of 25000 recalls

North Coast Medi-Tek Inc: Ultrasound probe cover, sterile. Catalog No. 910811.

Customer observed unsealed packages.

FDAJun 7, 2005OH• North Coast Medi-Tek Inc

Abbott Laboratories Medisense Products: Kroger Glucose Monitoring System; Recalling Firm/Manufact...

User may inadvertently change the Units of Measure from mg/dL to mmol/L and the blood glucose results could be misinterpreted. This may lead to under treatment and potential for hyperglycemia.

FDAJun 7, 2005IN• Abbott Laboratories Medisense Products

Abbott Laboratories Medisense Products: Tracker Blood Glucose Monitoring System; Recalling Firm/...

User may inadvertently change the Units of Measure from mg/dL to mmol/L and the blood glucose results could be misinterpreted. This may lead to under treatment and potential for hyperglycemia.

FDAJun 7, 2005

1...1196 119711981199 1200...1250

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• Abbott Laboratories Medisense Products

Abbott Laboratories Medisense Products: Easy Glucose Monitoring System; Recalling Firm/Manufactur...

User may inadvertently change the Units of Measure from mg/dL to mmol/L and the blood glucose results could be misinterpreted. This may lead to under treatment and potential for hyperglycemia.

FDAJun 7, 2005IN• Abbott Laboratories Medisense Products

Abbott Laboratories Medisense Products: SofTrac Glucose Monitoring System; Recalling Firm/Manufac...

User may inadvertently change the Units of Measure from mg/dL to mmol/L and the blood glucose results could be misinterpreted. This may lead to under treatment and potential for hyperglycemia.

FDAJun 7, 2005IN• Abbott Laboratories Medisense Products

Straumann Manufacturing Inc: RN synOcta Meso Abutment, crown margin 8.0mm, Ti Article:...

Basal screw is too short to adequately hold the dental abutment in the implant

FDAJun 6, 2005AZ, CA, DE +5 more• Straumann Manufacturing Inc

Redpoint Climbing Wall Descenders (MSA) – safety risk (2005)

Two types of descenders, which are used in recreational wall climbing, are included in this recall: Redpoint and Auto-Belay descenders. The descenders consist of a round metal housing into which a retractable red strap (Redpoint) or steel cable (Auto-Belay) is coiled. The front of each descender's round metal housing includes a red label (Redpoint) or green label (Auto-Belay) with the name of the product. A label on the back of the product's housing includes the descender's date of manufacture, last service date, and product number. Redpoint Descenders are identified with product numbers 10024873, 10027646 or 10027798. Auto-Belay Descenders are identified with the product number 10021806. Redpoint Descenders manufactured or serviced from August 27, 2004 through April 6, 2005 are included in the recall. Auto-Belay Descenders serviced from August 27, 2004 through April 6, 2005 are included in the recall.

CPSCJun 3, 2005Nationwide• Mine Safety Appliances Co. (MSA), of Pittsburgh, Pa.

DeWALT Framing Nailers – product defect (2005)

The recall involves new DeWALT D51844 and D51845 Heavy-Duty 20° Full Round Head Framing Nailers, and new DeWALT Model D51722 Heavy Duty 31° Clipped Head Framing Nailers. The recalled units have the following date codes: 200203, 20024, 200217, 200302, 200304, 200308, 200315, 200325, 200329, 200343, 200403, 200404, 200406, 200407, 200412, 200413, 200415, 200416 and 200417. The location of the date code is shown on the photograph below. The new units have a rework date code of 200449DM, 200450DM, 200451DM or 200452DM on the carton. The recall also involves reconditioned DeWALT D51844R and D51845R Heavy-Duty 20° Full Round Head Framing Nailers, and reconditioned DeWALT Model D51822R and D51823R Heavy Duty 31° Clipped Head Framing Nailers, with date codes 200423 through 200509. The date codes on all of the units are located in the area shown on the photograph below.

CPSCJun 3, 2005Nationwide• DeWALT Industrial Tool Co., of Baltimore, Md.

BioHorizons Implant Systems Inc One Perimeter Park South: The Maestor System 225-312, Profile Abutment for Cement, 5mm

The product labeled as a profile abutment for Cement contained a Straight Permucosal Ext, 5mm x 3mm.

FDAJun 3, 2005MI, PA, TX +1 more• BioHorizons Implant Systems Inc One Perimeter Park South

BioHorizons Implant Systems Inc One Perimeter Park South: The Maestro System 204-503, Straight Permucosal Ext, 5mm ...

The product labeled as a Straight Permucosal Ext, 5mm x 3mm contained a profile abutment for Cement.

FDAJun 3, 2005MI, PA, TX +1 more• BioHorizons Implant Systems Inc One Perimeter Park South

GVP Ceramic Hair Straightening Iron (Generic Value Products) – Fire Risk (2005)

Fire/Burn Risk

This hair straightening iron has a black housing with golden-colored ceramic heating plates. "Generic Value Products™" is written on the top of the iron and "GVP™" is written in a white circle on the side of the iron. The iron was packaged in a black and white box with the letters GVP™ in large type in the upper left hand front corner. The SKU is 264800, which is written on the packaging.

CPSCJun 2, 2005Nationwide• Generic Value Products, of Omaha, Neb.

Plenum Network Cables (Hitachi Cable) – Installation Defect (2005)

Fire/Burn Risk

The recalled cables typically were installed in data centers and other commercial applications. The part numbers for the recalled cables are 39419-50 (25-pair, category 5e); 30171-100 (50-pair, category 5e); and 30105-50 (25-pair, category 5). Only HCM brand cables with the following lot numbers are affected by this recall: AE589 and A4309 through A5551. The part number and lot number are printed on the jacket of the cables.

CPSCMay 31, 2005Nationwide• Hitachi Cable Manchester (HCM), Inc. of Manchester, N.H.

Northwest Medical Physics Equipment Inc: ISOLOC 4.2 Software Part Number NT-NW-425-520. Image gui...

When the ISOLOC (Version 4.2) profile distance unit is set to "centimeter" and the user clicked the "back" button in the digitizer window, the marker and target coordinates in the localization window erroneously display values ten times greater than the correct values.

FDAMay 31, 2005Nationwide• Northwest Medical Physics Equipment Inc

B. Braun Medical, Inc.: Locking Tear-Away Sheath Introducer Product Line. ACCUG...

Reports that the tearaway introducer sheaths have cracked hubs/handles and/or improper peeling of the sheath during use.

FDAMay 27, 2005IN• B. Braun Medical, Inc.

Toshiba American Med Sys Inc: Magnetic Resonance Imaging Systems; Visart, Excelart / E...

Patient information A is displayed with images for patient B.

FDAMay 25, 2005Nationwide• Toshiba American Med Sys Inc

B. Braun Medical, Inc.: Right Heart Catheter Product Line: Catalog Number 601129...

Reports in a small percentage of Right Heart Catheter Products Line related to cracked catheter tips, leaking at the manifold and cracked hubs.

FDAMay 25, 2005Nationwide• B. Braun Medical, Inc.

Radiometer America Inc: Package Insert which accompanies the Hematocrit and Metab...

The package insert, which accompanied the QC reagents used with ABL blood gas analyzers, referenced incorrect control ranges for Hct (hematocrit) testing. The range stated on the package insert was too low to generate accurate Hct test results (The control ranges were acceptable for the glucose and lactate testing).

FDAMay 24, 2005Nationwide• Radiometer America Inc

Toshiba American Med Sys Inc: Aplio Diagnostic Ultrasound System (SSA-700A and SSA-770A...

If the measurement mode is started from the Doppler mode and then the sweep speed setting is changed by the assigned user function, the measurement of the time direction results don't correspond to the actual values.

FDAMay 23, 2005Nationwide• Toshiba American Med Sys Inc

iBook PowerBook Batteries (Apple) – Overheating Risk (2005)

Fire/Burn Risk

The recalled lithium-ion batteries are used with the following computers: 12-inch iBook G4, 12-inch PowerBook G4 and 15-inch PowerBook G4. The recalled batteries include those with model numbers A1061, A1078 and A1079 and serial numbers that begin with HQ441 through HQ507 or 3X446 through 3X510. Consumers should remove the battery from the computer to view the model and serial numbers labeled on the bottom of the unit. No other PowerBook or iBook batteries are involved in this recall. Computer model name Battery model number Battery serial number range 12-inch iBook G4 A1061 HQ441 - HQ507 12-inch PowerBook G4 A1079 3X446 - 3X510 15-inch PowerBook G4 A1078 3X446 - 3X509

CPSCMay 20, 2005Nationwide• Apple Computer Inc., of Cupertino, Calif.

Carter Brothers Fun-Kart Go-Kart – Safety Issue (2005)

The recall includes one-seater models 1136-3020, 1136-3021, 1136-3420, 1136-3421, 1205-3020 and two-seater models 2336-3021, 2336-3022, 2336-5019, 2575-3020, 2575-3420, 2605-3416, 2605-3515, 2606-3016, 2606-3017, 2606-3416, 2606-3417, 2636-3016, 2636-3017, 2906-3015, 2906-3016, 2906-3017, 2906-4015, 2906-4016, 2906-4017, 2909-3015, 2909-3415, 2909-4015, 2910-3015, 2910-3016, 2910-3415, 2910-4015, 2910-4016, 2910-4415, 2911-4015, 2911-4016, 2946-3015, and 2946-3016. The model number and serial number are located under the seat (on the driver's side if two-seater). The Fun-Karts were produced in several colors, to include red, black, blue, purple and green.

CPSCMay 20, 2005Nationwide• Carter Brothers Manufacturing Co. Inc., of Brundidge, Ala.