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Newport Medical Instruments Inc

Newport Medical Instruments Inc Recalls

All product recalls associated with Newport Medical Instruments 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 22141–22160 of 25002 recalls

Newport Medical Instruments Inc: Newport HT50 Ventilator, Model # HT-50-H, HT50-HB, HT50-H...

The recall was initiated because Newport Medical has confirmed that the HT50 Dual Pac Ventilator is not compatiable with the external battery pack (p/n BAT3300A) supplied with the previous single battery ventilator. The Dual Pac system has a slightly higher amperage draw than the single battery and as a result can cause the fuse in the external battery pack to blow making the battery inoperable.

FDAJul 22, 2009Nationwide• Newport Medical Instruments Inc

Polaris ATVs (Polaris) – fire hazard (2009)

Fire/Burn Risk

This recall involves the Polaris ATVs with model year 2009. The ATVs were sold under market names Sportsman ESP XP 850 and Sportsman XP 850 ATVs. The model and serial number identification decal is located on the left side of the machine on the frame rail below the front fender. The following models are being recalled: Market Name Model Number Sportsman ESP XP 850 A09ZX85AG Sportsman XP 850 A09ZN85AL Sportsman ESP XP 850 A09ZX85AL Sportsman XP 850 A09ZN85AQ Sportsman ESP XP 850 A09ZX85AQ Sportsman XP 850 A09ZN85AS Sportsman ESP XP 850 A09ZX85AR Sportsman XP 850 A09ZN85AT Sportsman ESP XP 850 A09ZX85AS Sportsman XP 850 A09ZN85AX Sportsman ESP XP 850 A09ZX85AX Sportsman XP 850 A09ZN8XAL Sportsman ESP XP 850 A09ZX8XAG Sportsman XP 850 A09ZN8XAQ Sportsman ESP XP 850 A09ZX8XAL Sportsman XP 850 A09ZN8XAS Sportsman ESP XP 850 A09ZX8XAQ Sportsman XP 850 A09ZN8XAX Sportsman ESP XP 850 A09ZX8XAR Sportsman ESP XP 850 A09ZX8XAS Sportsman ESP XP 850 A09ZX8XAX

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CPSC

Jul 22, 2009

Nationwide

• Polaris Industries Inc., of Medina, Minn.

Elliptical Cross Trainers (Stamina) - Safety Instructions (2009)

This recall includes the following elliptical machines: Model Serial Number Magnetic 1772 Cross Trainer Elliptical Model No. 55-1772 08AUG000001-08AUG000360 08AUG000361-08AUG001078 08AUG002521-08AUG002878 08SEP001081-08SEP001438 08SEP001441-08SEP001798 08SEP002881-08SEP003238 08OCT001801-08OCT002158 08OCT002161-08OCT002518 08DEC003241-08DEC003598 Air 1725 Elliptical Cross Trainer Model No. 55-1725 08AUG000001-08AUG000596 08NOV000597-08NOV001192 09JAN000001-09JAN000596 Air Resistance 1723 Cross Trainer Model No. 55-1723 07SEP000001-07SEP001192 07OCT001193-07OCT001788 07DEC001789-07DEC002384 08JAN000001-O8JAN000596 08AUG000597-08AUG001192 08NOV001193-O8NOV001788 08DEC001789-08DEC002384 09JAN000001-09JAN000596 09MAR000597-09MAR001192 09MAY001193-09MAY001788

CPSCJul 21, 2009Nationwide• Stamina Products Inc. of Springfield, Mo.

Draeger Medical Systems, Inc.: Stabilet Infant Warming System, model numbers 200, 300, 1...

Fire/Burn Risk

Hot particles fell into the infant bassinet beneath a Radiant Infant Warmer. The resulting fire injured an infant. These devices are obsolete.

FDAJul 17, 2009Nationwide• Draeger Medical Systems, Inc.

Impac Medical Systems Inc: SEQUENCER component of MOSAIQ versions 1.30 (all builds),...

Potential for improper treatment. A software error may result in potential major underdosing to targeted areas from jaw blockage of the MLC aperture (jaw intrusion), and dosing to non-targeted areas from interstitial leaf leakage (jaw extrusion).

FDAJul 17, 2009AL, CA, CT +19 more• Impac Medical Systems Inc

Varian Medical Systems Oncology Systems: Varian Medical Systems, Eclipse Proton Convolution Superp...

Software Issue/Mistreatment Potential-- Due to software issues, dose distribution may be incorrect and unintended radiation doses may be delivered.

FDAJul 17, 2009IN, TX• Varian Medical Systems Oncology Systems

Angiodynamics, INC: SmartPort CT Port Access System, Catalog number CT80STPD,...

The product may contain an incorrect size catheter and introducer.

FDAJul 16, 2009AL, CA, CO +18 more• Angiodynamics, INC

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

Toshiba American Medical Systems Inc: Whole Body X--ray Scanner This device is indicated as a ...

1. It has been found that in raw data processing for Go&Return helical scanning, when the raw data acquired in the first scan (Go) and that acquired in the second scan (Return) are selected and reconstructed at one time, incorrect couch positions and scan times are displayed on the reconstructed images for the data acquired by Return scanning, while all related information is displayed on the reco

FDAJul 13, 2009Nationwide• Toshiba American Medical Systems Inc

Toshiba American Medical Systems Inc: Whole Body X--ray Scanner This device is indicated as ...

Class IIModerate

FDAJul 13, 2009Nationwide• Toshiba American Medical Systems Inc

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.

Lawn Tractors (Husqvarna) – Brake Failure (2009)

Laceration Risk

The recalled Craftsman power lawn tractor is gray colored, has 19.5 HP engine, automatic drive, and a 42 inch cutting deck. The following model and serial numbers are included in the recall. The model and serial numbers are located on a model plate under the tractor's seat. Models Craftsman 917.289080 Craftsman 917.289081 Serial Numbers 012709A001000 through 031209D999999

CPSCJul 8, 2009Nationwide• Husqvarna Consumer Outdoor Products N.A. Inc., of Augusta, Ga.

Mosquito Traps (BioSensory) – Laceration Risk (2009)

Fire/Burn Risk

The Dragonfly II Model 503 is a cylindrical unit made of metal and plastic with a black, silver and dark graphite finish. The units are about 36 inches tall and 8 inches in diameter. The Dragonfly logo, model number, electrical information, Canadian Standards Association (CSA) mark for Canada and the United States (C US), BioSensory street and internet address are engraved on the main housing, on the side opposite the control panel. The NightWatch Model 506 is a white molded plastic unit 14 inches long and 6 inches high with a black and white striped thermal lure over the top and sides. Two detachable pitfalls are on either side of the unit. The pitfalls have a felt ramp leading to the elongated collection pit. The NightWatch model number, electrical information, Canadian Standards Association (CSA) mark for Canada and the United States (C US), BioSensory street and internet address are engraved on the underside of the unit beneath the control panel.

CPSCJul 7, 2009Nationwide• BioSensory, Inc., of Putnam, Conn.