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Catheter Research, Inc

Catheter Research, Inc Recalls

All product recalls associated with Catheter Research, Inc.

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Recall Summary

Total Recalls

1000

Past Year

276

Class I (Serious)

242

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 3821–3840 of 4099 recalls

Catheter Research, Inc: Zinnanti Injector - 2.0; Size 2.0 mm, Length 23 cm, latex...

The uterine stop component was not included with the device.

FDAApr 24, 2006MN• Catheter Research, Inc

Emergency Smoke Hoods (EVAC) – Carbon Monoxide Risk (2006)

Fire/Burn Risk

These smoke hoods are one-time use respiratory devices that assist users with breathing, while escaping a fire. They include a transparent plastic hood that covers the user's head, and a canister that filters out toxic gases. "EVAC+™" or "EVAC-U8™" is printed on the canister.

CPSCApr 20, 2006Nationwide• Brookdale International Systems Inc., of Vancouver, British Columbia, Canada

Ski-Doo Snowmobiles (BRP) – Projectile Risk (2006)

The recall involves all models and packages of the Model Years 2005 and 2006 Mach Z and all models and packages of the Model Year 2006 MX Z Renegade 1000 Ski-Doo® snowmobiles. The Mach Z model was available in black and the MXZ model was available in black or yellow. Model name is located on the side panels.

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CPSCApr 3, 2006Nationwide• Bombardier Recreational Products Inc. (BRP), of Quebec, Canada

American Girl Children's Jewelry – Lead Poisoning (2006)

The recall includes American Girl necklaces, bracelets, earrings and hair accessories for girls. The recall does not include jewelry for American Girl dolls. The jewelry's packaging features a red and white cardboard backing with "American Girl" and "Made in China" written on the front.

CPSCMar 30, 2006Nationwide• American Girl Inc., of Middleton, Wis., a division of Mattel Inc., of El Segundo, Calif.

Plasma Flat Panel TVs (Philips) – Potential Defect (2006)

The recall involves only certain 42- and 50-inch, 2005 model Philips branded Plasma Flat Panel Televisions with Ambilight technology, which is an ambient lighting feature that projects a soft light onto the wall behind the TV to enhance the display. They were manufactured with the following model, date codes, and serial numbers: Model Display Type Production Began Production Ended Beginning Serial Range Ending Serial Range 42PF9630A/37 Plasma April 2005 July 2005 AG1A0518xxxxxx AG1A0528xxxxxx 50PF9630A/37 Plasma May 2005 August 2005 AG1A0519xxxxxx AG1A0533xxxxxx 50PF9630A/37 Plasma June 2005 August 2005 YA1A0523xxxxxx YA1A0534xxxxxx 50PF9830A/37 Plasma June 2005 August 2005 AG1A0526xxxxxx AG1A0533xxxxxx The model and serial numbers can be found on the back of the TV on the label that looks like the example in the picture: The serial number can also be obtained by pushing the following keystrokes on the remote control: 123654, after which a customer service menu ("CSM") will be displayed on the screen. In the menu, line 03 displays the type number and line 04 displays the production code (identical to the serial number of the set). Press the MENU button on the remote to exit the CSM.

CPSCMar 16, 2006Nationwide• Philips Consumer Electronics North America, of Atlanta, Ga.

Karl Storz Endoscopy America Inc 600 Corporate Pointe: Storz Documentation Cart with Articulating Arm, Model Num...

THE ARTICULATING ARM ON THE CART, WHICH HOLDS THE MONITOR, MAY FALL OFF FROM THE CART DURING MANIPULATION. WHEN IT FALLS, IT COULD HIT THE GROUND OR FALL ON THE PEOPLE/OBJECTS THAT ARE IN CLOSE PROXIMITY.

FDAMar 10, 2006Nationwide• Karl Storz Endoscopy America Inc 600 Corporate Pointe

Instrumentation Laboratory Co.: HemosIL RecombiPlasTin. Prothrombin Time Test. Each Recom...

Firm received 2 complaints concerning incorrect prothrombin time (PT) results while using the reagents on samples of patients taking the antibiotic CUBICIN (Daptomycin for injection).

FDAMar 7, 2006Nationwide• Instrumentation Laboratory Co.

Instrumentation Laboratory Co.: Hemoliance RecombiPlasTin. Prothrombin Time Test. The pro...

Firm received 2 complaints concerning incorrect prothrombin time (PT) results while using the reagents on samples of patients taking the antibiotic CUBICIN (Daptomycin for injection).

FDAMar 7, 2006Nationwide• Instrumentation Laboratory Co.

Quechua Snowboard Bindings – Fall Risk (2006)

The model Rn'x7FX Quechua snowboard bindings are white or black. The word "Quechua" is located on the back of the binding. The model number is stamped on the box. Other Quechua snowboard bindings are unaffected by the recall but consumers may bring them to the store for proper identification.

CPSCMar 3, 2006Nationwide• Decathlon USA, of Wilmington, Mass.

Integrated Orbital Implants Inc: Bio-Eye Hydroxyapatite (HA) Orbital Implant and Conformer...

The end label on the outer box was mislabeled on 9 of a 10 unit lot. The end label says ''22 mm'' and the implants are actually ''20 mm''. The main label on the cardboard box applied by the contract packager is correct in identifying the product as ''20 mm''.

FDAFeb 27, 2006Nationwide• Integrated Orbital Implants Inc

GE Medical Systems Information Tecnology 9900 Inovation Drive RP 2122 3rd Floor Wauwatosa WI 53226: Datex-Ohmeda S/5 Critical Care Monitor with L-CICU01, L...

GE Healthcare (Datex-Ohmeda) S/5 Critical Care Monitor and S/5 Compact Critical Care Monitor with L-CICU01, L-CICU02A, L-ICU05 & L-ICUO5A software had an issue where the Heart Rate (HR) was displaying as ---(3 dashes) when the monitor was used continuously for 49 days without a cold start. A missed alarm or missed HR value could cause a delay in recognition of a cardiac event that may result i

FDAFeb 6, 2006IA, PR• GE Medical Systems Information Tecnology 9900 Inovation Drive RP 2122 3rd Floor Wauwatosa WI 53226

GE Medical Systems Information Tecnology 9900 Inovation Drive RP 2122 3rd Floor Wauwatosa WI 53226: Datex-Ohmeda S/5 Compact Critical Care Monitor with L-CIC...

FDAFeb 6, 2006IA, PR• GE Medical Systems Information Tecnology 9900 Inovation Drive RP 2122 3rd Floor Wauwatosa WI 53226

International Technidyne Corp: Tenderlett Adult Lancet, sterile, single use. Red trigge...

Some packages contained a pin-hole defect that permitted the transmission of dye through the primary packaging. This is a sterile product.

FDAJan 23, 2006Nationwide• International Technidyne Corp

Boy's Windbreaker Jacket (Hurley) – Drawstring Danger (2006)

The recalled jackets are black or gray and were sold in youth sizes up to size 20. "HurleyCo" is stitched on the upper left outside of the jacket. The style number BJ06GS is printed on a label sewn inside the left side seam of the jacket.

CPSCJan 12, 2006Nationwide• Hurley International, of Costa Mesa, Calif.

Ski-Doo Snowmobiles (Bombardier) – Additional Model Defect (2006)

The recall involves certain Ski-Doo Model Year 2006 REV500 SS, REV 600 HO, and REV 600 HO SDI snowmobiles. For a complete list of model numbers and serial numbers affected by this recall please log onto www.ski-doo.com The model number and serial number can be found on the tunnel. Year Model Package Model Number 2006 MX Z Adrenaline 000BE6C00 000BE6D00 000BE6E00 000BE6F00 000BF6C00 000BF6D00 2006 MX Z Trail 000BH6B00 2006 MX Z Renegade X 000BW6C00 2006 GSX Sport 000DC6A00 000DC6B00 2006 GTX Sport 000ED6A00 000ED6B00 000ED6C00 000EJ6A00 000EJ6B00 2006 GTX Ltd 000EH6B00

CPSCJan 5, 2006Nationwide• Bombardier Recreational Products Inc., of Valcourt, Quebec

Ski-Doo Snowmobiles (Bombardier) – Vehicle Safety Concern (2006)

The recall involves certain Ski-Doo Model Year 2006 snowmobiles. The platforms involved are the REV, RT, and RF. For a complete list of model numbers and serial numbers affected by this recall please log onto www.ski-doo.com Check the owner's manual for the location of the model number and serial number. Most are located on the tunnel. Year Model Package Model Number 2006 MX Z Adrenaline 000BD6A00 000BD6B00 000BD6C00 000BD6D00 000BD6E00 000BD6F00 000BE6A00 000BE6B00 000BE6C00 000BE6D00 000BE6E00 000BE6F00 000BF6A00 000BF6B00 000BF6C00 000BF6D00 000BL6A00 000BL6B00 000BL6C00 000BL6D00 000BL6E00 000BL6F00 2006 MX Z Trail 000BH6A00 000BH6B00 000BH6C00 2006 MX Z Fan 000BP6A00 000BR6A00 000BR6B00 2006 MX Z Renegade 000BU6A00 000BU6B00 000BU6C00 000BU6D00 000BX6A00 000BX6B00 000BX6C00 000BX6D00 2006 Summit Highmark 000CD6A00 000CD6B00 000CE6A00 000CE6B00 000CE6C00 2006 Summit Adrenaline 000CJ6A00 000CJ6B00 000CJ6C00 000CK6A00 000CK6B00 000CL6A00 000CL6B00 000CL6C00 2006 Summit Fan 000CM6A00 000CM6B00 2006 GSX Ltd 000DA6A00 000DA6B00 000DD6A00 000DD6B00 2006 GSX Sport 000DC6A00 000DC6B00 000DE6A00 000DE6B00 2006 GSX Fan 000DF6A00 000DG6A00 2006 GTX Ltd 000EA6A00 000EA6C00 000EH6A00 2006 GTX Sport 000ED6A00 000ED6B00 000ED6C00 000EJ6A00 000EJ6B00 000EJ6C00 2006 GTX Fan 000EL6A00 000EL6B00 000EL6C00 000EM6A00 000EM6B00 000EM6C00 2006 Expedition Sport 000EN6A00 000EN6B00 2006 Skandic Tundra 000GA6A00 000GA6B00 000GA6C00 2006 Freestyle Freestyle 000GB6A00 000GB6B00 000GB6D00 000GB6E00 000GB6F00

CPSCJan 5, 2006Nationwide• Bombardier Recreational Products Inc., of Valcourt, Quebec

Abbott Laboratories Diagnostic Div: Clinical Chemistry Multiconstituent Calibrator--- List nu...

The two Multiconstituent Calibrator (MCC) lot numbers 19906M200 and 20879M100 failed to meet product performance expectations throughout the labeled expiration period, as a result of the shortened expiration dating, two lots are now expired. The expiration date for Lot number 26674M100 will be revised from 2006-07-31 to 2006-01-31.

FDADec 23, 2005Nationwide• Abbott Laboratories Diagnostic Div

Scarpa T2X Telemark Ski Boots – Potential Defect (2005)

The two recalled models of T2X Telemark ski boot can be identified by a dual color ankle cuff and the marking T2X on the outside of each boot (boxes are marked with model numbers: 142045 Men's and 142046). Repaired or replaced product can be identified by a single color cuff: Men's cuffs are red, women's cuffs are blue.

CPSCDec 16, 2005Nationwide• Calzaturifico S.C.A.R.P.A. S.P.A., of Italy

Instrumentation Laboratory Co.: GEM PREMIER 3000

Software error may report higher results for glucose and lactate

FDADec 16, 2005Nationwide• Instrumentation Laboratory Co.

Ceramic Teapots (Starbucks) – Product Safety (2005)

Fire/Burn Risk

This recall involves 40-ounce white ceramic teapots with bamboo handles. The phrase "Microwave and Dishwasher Safe" is printed on the bottom of each teapot.

CPSCNov 28, 2005Nationwide• Starbucks Coffee Company, of Seattle, Wash.