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Linvatec Corp. dba ConMed Linvatec

Linvatec Corp. dba ConMed Linvatec Recalls

All product recalls associated with Linvatec Corp. dba ConMed Linvatec.

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Recall Summary

Total Recalls

1000

Past Year

442

Class I (Serious)

138

Most Recent

Dec 2025

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 6881–6900 of 7663 recalls

Linvatec Corp. dba ConMed Linvatec: ST ULTRAPOWER DIAMOND WHEEL (RED) 25.4mm, Catalog Number...

ConMed Linvatec is recalling Ultrapower Bur, Diamond Wheel for possibility of a packaging breach in the sterile barrier.

FDAJul 31, 2009Nationwide• Linvatec Corp. dba ConMed Linvatec

Linvatec Corp. dba ConMed Linvatec: PowerProMax PRO5100M Battery Single Trigger, PowerProMax...

There is a potential the devices may self activate for their PowerPro, PowerProMax, and MPower I Handpieces manufactured prior to June 1, 2008.

FDAJul 31, 2009Nationwide• Linvatec Corp. dba ConMed Linvatec

Davol, Inc., Sub. C. R. Bard, Inc.: BARD Simpulse" SOLO System with Soft Splash Shield Tip P...

Product sterility may be compromised due to lack of package integrity.

FDA

1...343 344345346 347...384

Page 345 of 384Next

Jul 30, 2009

Nationwide

• Davol, Inc., Sub. C. R. Bard, Inc.

Purdy 2½" 4-Edge Scrapers (Allway Tools) – laceration risk (2009)

Laceration Risk

The recalled scraper is a 2 ½" wide steel tool with a four-sided edge. The handle has a soft black grip with "Purdy" printed in red letters on the side of the handle.

CPSCJul 30, 2009Nationwide• Allway Tools Inc., of Bronx, New York

Cyberonics, Inc: Cyberonics VNS Therapy Programming M250 Programming Syste...

Some VNS Therapy System replacement Demipulse generators reporting low lead impedance readings. In rare instances, a system diagnostic test using Model 250 Programming Software (versions 7.1 and earlier) may report "Lead Impedance: OK" when a short-circuit condition exists.

FDAJul 24, 2009PR• Cyberonics, Inc

Spacelabs Healthcare, Incorporated: Spacelabs Medical Integrated ECG Cable are supplied as pa...

The Spacelabs Medical Integrated ECG Cables, PN: 700-0008-22, 700-0008-23, 700-0008-24, and 700-0008-25 will not withstand the high voltage of a defibrillation shock.

FDAJul 23, 2009Nationwide• Spacelabs Healthcare, Incorporated

Switch-A-Roo Telephone Toys (Evenflo) - Choking Risk (2009)

Choking Hazard

The recall involves Evenflo Switch-A-Roo telephone toys made between October 2008 and June 2009. The model number is 6391911.

CPSCJul 16, 2009Nationwide• Evenflo Co. Inc., of Miamisburg, Ohio

Leonhard Lang Gmbh Archenweg 56 Innsbruck Austria: S&W Electrodes for Defibrillation, 10 Defibrillation Elec...

A potential risk was identified associated with the connectors of the defibrillation electrodes DF20. It was found that some of the connectors do not slip easily into the sockets of the defibrillator or an extension cord of the defibrillator. In such cases increased force or some wiggling is required to insert the connector fully. A potential risk for patients exist, if (a) such a connector (b)

FDAJul 10, 2009FL• Leonhard Lang Gmbh Archenweg 56 Innsbruck Austria

Leonhard Lang Gmbh Archenweg 56 Innsbruck Austria: SKINTACT Electrodes for Defibrillation, 10X REF DF20, Rx ...

FDAJul 10, 2009FL• Leonhard Lang Gmbh Archenweg 56 Innsbruck Austria

Kidde Smoke Alarms (Walter Kidde) - Fire Warning Failure (2009)

Fire/Burn Risk

This recall involves Kidde dual sensor smoke alarms model PI2000. The alarms can be identified by two buttons, "HUSH" and "PUSH AND HOLD TO TEST WEEKLY," which are located on the front/center of the alarm. The model number and date code are on the back of the smoke alarm. Only date codes 2008 Aug.01 through 2009 May 04 are included in this recall.

CPSCJul 9, 2009Nationwide• Walter Kidde Portable Equipment Inc., of Mebane, N.C.

Rope Cutters (MarineTech) – Fire Risk (2009)

Fire/Burn Risk

The recalled tabletop rope cutters are used for cutting and cauterizing rope. This recall includes MarineTech part number 75-7070 and West Marine part number 559419. The Marine Tech part number is located on the side of the rope cutter. "Panther" is printed on the rope cutter.

CPSCJul 1, 2009Nationwide• MarineTech Products Inc., of White Bear Lake, Minn.

Bausch & Lomb Inc: Bausch & Lomb, Boston Conditioning Solution, Original For...

The product failed to meet one of the shelf life specifications at the end of the expiry period.

FDAJun 30, 2009Nationwide• Bausch & Lomb Inc

Spacelabs Healthcare, Llc: Blease Sirius Anaesthesia System is a anaesthesia Gas Mac...

Users may experience difficulty turning the control knob to an active vapour delivery setting, or may not be able to turn on the Left Hand mounted vapouriser on the Blease Sirius Anaesthesia Systems.

FDAJun 25, 2009IN, LA, SD• Spacelabs Healthcare, Llc

Bath Tubs (Crane) – Drowning Risk (2009)

The bathtubs are acrylic with 6-12 jets. The Crane logo is printed on the whirlpool and/or noted on the air control valve.

CPSCJun 23, 2009Nationwide• Crane Plumbing LLC, of Dallas, Texas

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: POWERSAIL Coronary Dilatation Catheter: 3.25x18mm (US) Pa...

Distal shaft of the POWERSAIL coronary Dilatation Catheters exhibits damage that may result in a leak of contrast material and functional failures.

FDAJun 17, 2009Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

St. Jude Medical Atrial Fibrillation Division Inc: St. Jude Medical Epicor UltraWand LP Handheld Ablation De...

The firm states that overheating of cardiac tissue is caused by inadequate cooling. The potential exists when the UltraWand is run using off-label cooling methods (gravity saline flow instead of pump) that cooling flow to one or both cells can be decreased based on pressure applied by the physician to the device. To reflect this information to the user, the Atrial Fibrillation Division (AFD) has

FDAJun 15, 2009AL, AZ, CA +33 more• St. Jude Medical Atrial Fibrillation Division Inc

Cardinal Health 303 dba Cardinal Health: Alaris Pump Module, Model 8100.

There is a potential risk of over infusion when certain fluids solidify in the pumping mechanism of the Alaris Pump module. This notification is to reinforce the importance of proper techniques for IV set loading and cleaning. When IV sets are improperly loaded, the set can tear and cause medication to leak and potentially enter the bezel area. Improper cleaning of the device, such as using hig

FDAJun 12, 2009PR• Cardinal Health 303 dba Cardinal Health

Cardinal Health 303 dba Cardinal Health: The Alaris PC Unit, Model Numbers 8000 and 8015 (formerly...

There is a potential risk for medication not being delivered when IV tubing sets are occluded in the Alaris Pump module. This can occur if IV sets are set up in the infusion pumps but not used for an extended period of time. If users fail to clear the occlusion, then the occluded tubing may cause medication not to be delivered. A delay of medication may result in serious injury and/or death, an

FDAJun 12, 2009PR• Cardinal Health 303 dba Cardinal Health

Cardinal Health 303 dba Cardinal Health: The Alaris PC Unit, Model 8015 (manufactured or serviced ...

There is a potential in the specified ESD (electrostatic discharge) protection circuitry in the keypad of Alaris PC units manufactured or serviced between April 2008 through January 2009. In these units there is a potential for the keypad not being responsive, key entries without key presses, or key entries that register incorrectly which may result in an over-infusion or under-infusion. An over

FDAJun 12, 2009PR• Cardinal Health 303 dba Cardinal Health

Cardinal Health 303 dba Cardinal Health: The Alaris PC Unit, Model Numbers 8000 and 8015 (formerly...

Affected Unit: Alaris PC Unit (Models 8000 and 8015) with software a versions 8 and above when used with the Alaris PCA module (Model 8120) There is a potential risk of over infusion related to a warning message on the user interface of the Alaris PC unit when used in conjunction with the Alaris PCA module. When the Alaris PC unit detects a programmed infusion for the Alaris PCA module that exceed

FDAJun 12, 2009PR• Cardinal Health 303 dba Cardinal Health