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Enpath Medical, Inc

Enpath Medical, Inc Recalls

All product recalls associated with Enpath Medical, 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 23501–23520 of 25000 recalls

Enpath Medical, Inc: Angel Medical Systems Lead Adaptor system adapts a St. Ju...

The internal component (Connector Block) of the Lead Adapter used to secure a lead to the adapter has exhibited varying degress of radial cracks that could cause a temporary intermittent electrical signal disruption if lateral tension is applied to device.

FDAJul 18, 2006CA, MN, NJ• Enpath Medical, Inc

Konica Minolta Medical Imaging USA, Inc.: Regius Model 370 Digital Radiography Konica Minolta

A hand grip column, even though locked in position, moved downward about 3 cm while a patient was holding the hand grip for lateral exposure. When the hand grip moved down, the patient who was holding it lost his or her balance and almost fell. This problem only occurred in Japan with one system.

FDAJul 14, 2006TX• Konica Minolta Medical Imaging USA, Inc.

Disetronic Medical Systems, Inc.: Disetronic D-TRONplus Insulin Pump Battery Pack; Ref/Cata...

The battery may turn the pump off without warning due to a design change in the battery.

1...1174 117511761177 1178...1250

Page 1176 of 1250Next

FDAJul 13, 2006Nationwide• Disetronic Medical Systems, Inc.

Ryobi Radial Arm Saws (Ryobi) – Blade Detachment Risk (2006)

Laceration Risk

The recall involves all RA200 and RA202 radial arm saws. These are bench top models with 8¼-inch blades. Each unit has a data plate immediately behind the operator grip for the saw, which says "RYOBI 8 1/4" Radial Arm Saw" and either "RA200" or "RA202."

CPSCJul 13, 2006Nationwide• Ryobi Motor Products Corp. formerly of Anderson, S.C. ("RMP")

Bicycle Headsets (M2Racer) – Fall Hazard (2006)

The headset is the component on a bicycle, which provides a interface that can rotate between the bicycle fork and the bicycle frame itself. The Conventional Headset is constructed of an anodized black alloy housing, stainless steel, and polymers. The Integrated Lite Headset is constructed of a black polymer housing and light weight alloys. The Integrated Headset weighs 29 grams; the Conventional Headset weighs 39 grams.

CPSCJul 12, 2006Nationwide• M2Racer LLC, of Burlingame, Calif.

Lawn Tractors (Husqvarna) – Fire Hazard (2006)

Fire/Burn Risk

The lawn tractors were sold under the Husqvarna, Craftsman, Poulan Pro, Poulan, Weed Eater, Southern States and Murray brand names. Recalled tractors' product, model and serial numbers are listed in the chart below. To determine if a tractor is included in the recall, check the lawn tractors' product, model and serial numbers, located on a label under the seat of the tractor. Brand Product Number Model Number Serial Number Range Service Center Craftsman® NA 917.27662 917.27663 917.27618 917.27664 120905-X00XXXX through 061606-X00XXXX (800) 659-5917 Monday through Saturday between 6 a.m. and 8 p.m. ET. www.sears.com NA 917.27535 917.27639 917.27640 917.27641 917.27678 090905-X00XXXX through 062206-X00XXXX Husqvarna® 960430003 00 YT1942T 120905-X00XXXX through 061606-X00XXXX (866) 721-6091 Monday through Friday between 8 a.m. and 5 p.m. ET www.husqvarna.com 960130019 00 LT16542 090905-X00XXXX through 062206- X00X`XXX Murray 960120058 00 960120059 00 MB12538LT MB1842LT 120905-X00XXXX through 061606-X00XXXX (866) 284-8872 Monday through Friday between 8 a.m. and 5 p.m. ET Poulan® 960420026 00 C20H42YT 120905-X00XXXX through 061606-X00XXXX (866) 284-8872 Monday through Friday between 8 a.m. and 5 p.m. ET www.poulan.com 960120043 00 960120044 00 960120044 01 960120044 02 960120045 00 960120045 01 960120053 00 960170004 00 PO12538LT PB1638LT PB1638LT PB1638LT PB1842LT PB1842LT PB185H42LT PB18H42LT 090905-X00XXXX through 062206-X00XXXX Poulan Pro® 960420020 00 960420008 00 960420009 00 960420016 00 PB19H42YT PB20H42YT PK20H42YT XT19H42YT 120905-X00XXXX through 061606-X00XXXX (866) 284-8872 Monday through Friday between 8 a.m. and 5 p.m. ET www.poulan.com 960160013 00 960160013 01 960120060 00 HD17542 HD17542 XT185H42LT 090905-X00XXXX through 062206-X00XXXX Southern States 960420011 00 SO20H42YT 120905-X00XXXX through 061606-X00XXXX (866) 284-8872 Monday through Friday between 8 a.m. and 5 p.m. ET 960120054 00 960120055 00 960120057 01 SO1638LT SO17542LT SO19H42LT 090905-X00XXXX through 062206-X00XXXX Weed Eater® 960160014 00 960160014 02 HD13538 090905-X00XXXX through 062206-X00XXXX (866) 284-8872 Monday through Friday between 8 a.m. and 5 p.m. ET www.weedeater.com

CPSCJul 11, 2006Nationwide• Husqvarna Outdoor Products Inc., of Augusta, Ga., formerly known as Electrolux

Richard Wolf Medical Instruments Corp.: Tubing Set for TEM-Combined System; the tube set consists...

The irrigation tubing in the tube set was assembled incorrectly with the connectors reversed.

FDAJul 7, 2006Nationwide• Richard Wolf Medical Instruments Corp.

Wako Chemicals, USA Inc: Lp(a) Calibrator, Cat No. 998-41491, 1 ml glass bottles, ...

Unexpected low cholesterol results-The Cholesterol calibrator (Lp(a)) component of the in vitro diagnostic kit for cholesterol testing, has provided patient results lower than the correct value.

FDAJul 6, 2006Nationwide• Wako Chemicals, USA Inc

Oasis Medical Inc: OASIS Medical SOFT PLUG Extended Duration Plug, Reference...

Labeled with an incorrect diameter

FDAJul 6, 2006Nationwide• Oasis Medical Inc

Radiometer America Inc: Radiance Data Management System, Software Version 2.60, m...

Incorrect FI02 values: programming issue can cause incorrect values to be transmitted to the LIS when : 1)- The FIO2 result is edited in the manual sample processing mode--2)- An existing result is opened and FI02 is then edited and sent.....In both cases RADIANCE will transmit the original FI02 value, not the value that was edited.

FDAJul 6, 2006CO, IN, MO• Radiometer America Inc

Lexar JumpDrive (Lexar) – Burn Hazard (2006)

Fire/Burn Risk

The recalled drives are high speed flash drives used to store, transfer and carry data from one computer to another. This recall only includes Lexar JumpDrive® FireFly which is sold in various colors, and Lexar JumpDrive® Secure II 1GB which has a metallic silver housing. "Lexar" is embossed on the front of the plastic housing and the capacity is marked on the back. The part number is located on the FireFly's packaging, and on the back of the Secure II 1GB drive. JumpDrive® FireFly Capacity Part Number 256MB (red) JDFF256-431RU JDFF256-264 JDFF256-445RU 512MB (lime green) JDFF512-431EM 1GB (blue) JDFF1GB-431TO 2GB (black) JDFF2GB-431BK JumpDrive® Secure II 1GB Part Number JDSE1GB-00-500 Rev H and 3052-1GBA-2006 JDSE1GB-00-500 Rev H and 3052-1GBA-2106 JDSE1GB-00-500 Rev H and 3052-1GBA-1906 JDSE1GB-00-500 Rev H and 3052-1GBA-1806

CPSCJul 6, 2006Nationwide• Lexar Media Inc., of Fremont, Calif.

Paloma Rattles (Tiffany) – Safety Hazard (2006)

Laceration Risk

The Paloma Rattle is a ring that is 2.5 inches in diameter. It consists of nine linked sterling-silver balls that contain small beads.

CPSCJul 5, 2006Nationwide• Cunill Orferbres, of Barcelona, Spain, for Tiffany and Company, of New York, N.Y.

Heat & Glo Twilight Fireplaces (Heat & Glo) – Fire Risk (2006)

Fire/Burn Risk

The recall involves the Heat & Glo Twilight II and IIB indoor/outdoor see-through gas fireplaces. The model name, Twilight II or IIB, can be found by looking at the bottom right side of the inside of the control compartment of the inside portion of the fireplace.

CPSCJul 5, 2006Nationwide• Heat & Glo, of Lakeville, Minn.

Philips Medical Systems North America Co. Phillips: Easy Vision Workstation Family (for the manipulation and ...

Potential for measurements, lines, texts, etc to be stored incorrectly.

FDAJul 1, 2006Nationwide• Philips Medical Systems North America Co. Phillips

MRL, Inc., A Welch Allyn Company: Welch Allyn PIC 50 Portable Intensive Care System Multi-P...

The Welch Allyn PIC 50 Defibrillators may display a 'Defib Comm' or 'Pace Comm' error message on the device display during use which may result in a terminal failure of the device to analyze the patient's ECG and deliver the appropriate therapy.

FDAJun 30, 2006PR• MRL, Inc., A Welch Allyn Company

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1 Roller Pump 6 inch dia...

The roller pump speed control knobs and the centrifugal pump speed control knobs may fail to function/change pump speed.

FDAJun 30, 2006Nationwide• Terumo Cardiovascular Systems Corp

Radiometer America Inc: SafeClinitubes, Capillary caps (purple), 905-787. The de...

Leaking Capillary Caps- The dimensions and shapes of the capillary caps do not fit the capillary tubes correctly. This can cause the capillary tubes to leak.

FDAJun 29, 2006Nationwide• Radiometer America Inc

Hardy Media Inc Dba Hardy Diag: BHI Agar with Vancomycin, for in vitro diagnostic use. C...

This recall is being conducted due to the performance failure nearing the end of the product shelf life.

FDAJun 27, 2006Nationwide• Hardy Media Inc Dba Hardy Diag

Enpath Medical, Inc.: Channel Steerable Sheath in 8F Enpath part # 10775-003, B...

Enpath has become aware that some of the Enpath Medical 8F & 9F Steerable sheath devices may have a non-conforming flushport bond that causes a leak where air may enter the flush port chamber.

FDAJun 27, 2006CA, MA• Enpath Medical, Inc.

Terumo Cardiovascular Systems Corp: TERUMO KHURI MYOCARDIAL PH MONITORING SYSTEM, CATALOG NUM...

Lack of Assurance of Sterility: these specific lots of sensors lack supporting documentation for sterilization assurance.

FDAJun 23, 2006Nationwide• Terumo Cardiovascular Systems Corp