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Angiomed Gmbh Wachhausstrasse 6 Karlsruhe Germany

Angiomed Gmbh Wachhausstrasse 6 Karlsruhe Germany Recalls

All product recalls associated with Angiomed Gmbh Wachhausstrasse 6 Karlsruhe Germany.

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Recall Summary

Total Recalls

1000

Past Year

620

Class I (Serious)

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 10261–10280 of 10937 recalls

Angiomed Gmbh Wachhausstrasse 6 Karlsruhe Germany: Bard Luminexx Endoscopic Biliary Stent and Delivery Syste...

Biliary Stents may malfunction and cause failure to expand, fracture, incomplete deployment, inaccurate positioning, migration, or lumen perforation.

FDAJul 28, 2005Nationwide• Angiomed Gmbh Wachhausstrasse 6 Karlsruhe Germany

Boston Scientific Marlbourgh: Adapter for ACMI Hysteroscope Catalog Number: 55035

The Hysteroscope Adapter used with the HTA System may disassemble and result in a fluid leak.

FDAJul 28, 2005CA, DE, FL +9 more• Boston Scientific Marlbourgh

Philips Medical Systems North America Co. Phillips: Interis Allura BiPlane X-Ray System

1) During positioning of the Lateral Stand the rotation and/or skew movement may travel unexpectedly in opposite direction; 2) movement may be faster than normal speed; 3) the stand may not stop immediately upon release of the joystick.

1...512 513514515 516...547

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FDAJul 27, 2005Nationwide• Philips Medical Systems North America Co. Phillips

Terumo Cardiovascular Systems Corp: Terumo/Capiox Cardiovascular Kit containing the CAPIOX Di...

Small cracks in the blood chamber may allow air to enter the rotor of the device

FDAJul 26, 2005AZ, CA, IL +5 more• Terumo Cardiovascular Systems Corp

Industrial Fire Extinguishers (Kidde) – Valve Malfunction (2005)

Fire/Burn Risk

This Alert involves all Kidde 10 lb. dry chemical fire extinguishers manufactured with a black plastic Zytel® nylon valve assembly and a steel cylinder, between 1991 and 2000. These units were the subject of Kidde Service Bulletin 007 issued on July 21, 2004. These units were designed for commercial and industrial applications, and the majority of these units were placed into service in factories, plants, businesses and other commercial locations, as they require service by a qualified Fire Extinguisher Distributor or Service Organization every 6 years. Some of these units are in use in residential settings. The affected extinguishers have a steel cylinder with a welded neck ring and are between 19 to 21 inches tall, as depicted in the image below. This Alert does not apply to Kidde's smaller 2 1/2 and 5 lb. residential fire extinguishers.

CPSCJul 26, 2005Nationwide• Walter Kidde Portable Equipment Inc., of Mebane, N.C.

Boston Scientific CRM Corp: CONTAK RENEWAL 3 AVT model numbers M150 and M155; CONTAK ...

Guidant is revising its original recommendations set forth in the 06/17/05 physician letter because new information indicates that one of the original recommendations can increase the risk of a latching event, which may limit available therapy.

FDAJul 25, 2005IN• Boston Scientific CRM Corp

Boston Scientific CRM Corp: VITALITY AVT, model A135 and A155. Implantable Cardiover...

FDAJul 25, 2005IN• Boston Scientific CRM Corp

Boston Scientific CRM Corp: VENTAK PRIZM AVT model no. 1900, Atrial and Ventricular T...

FDAJul 25, 2005IN• Boston Scientific CRM Corp

Tiki Cone Metal Torch – Fire Safety Risk (2005)

Fire/Burn Risk

The recalled Tiki® Cone Metal Torch is a 6-foot-long outdoor open-flame lamp consisting of a black metal pole topped by a copper-colored, cone-shaped metal head. A black decorative rod spirals around the head of the torch. The torch head includes the fuel reservoir, cover and wick. It was sold under Lamplight Farms model numbers 1263 and 126301 and Wal-Mart item numbers 1656121 and 1691366. Both items were sold with the same UPC number 086861012635, which is located on the bottom of the printed hangtag.

CPSCJul 19, 2005Nationwide• Lamplight Farms Inc., a Division of W.C. Bradley Company, of Menomonee Falls, Wis.

GE Medical Systems Information Technologies: GE Healthcare Centricity Cardiology AI1000 Workstation ve...

The potential exists for the AI1000 workstation to mix images from one study with images from another study. Mixed studies could be from the same patient or from different patients. Mixed patient images could compromise patient condition or diagnosis and treatment.

FDAJul 18, 2005AL, AZ, AR +38 more• GE Medical Systems Information Technologies

Sammons Preston Rolyan, An Ability One Company: TM-300 Traction System; an Rx software driven device used...

The traction device may malfunction, producing oscillation and a jerking motion.

FDAJul 13, 2005Nationwide• Sammons Preston Rolyan, An Ability One Company

Medtronic Emergency Response Systems, Inc.: Hard shell carry case for the LIFEPAK 500 AED.

Some hard shell carry case for LIFEPAK 500 and LIFEPAK CR Plus automated external defibrillators may have blocked pressure vent which may make it difficult to open the case after a sudden decrease in altitude (such as in aircraft landng or mountain descent).

FDAJul 12, 2005Nationwide• Medtronic Emergency Response Systems, Inc.

Nature's Bounty Multivitamins – Contamination Risk (2005)

The Nature's Bounty and Natural Wealth brand multivitamins have lot number 60835-06 written on the label. The recalled vitamins were sold in containers of 100 caplets. The containers are both clear with white caps. They are labeled "Nature's Bounty Multi-Day Multivitamin Plus Iron" or "Natural Wealth Daily Vitamin Plus Iron."

CPSCJul 12, 2005Nationwide• NBTY Inc., of Bohemia, N.Y.

Becton Dickinson & Company: BD Vacutainer Blood Transfer Device. It consists of a Lu...

Customer complaints state the needle had separated from the hub, resulting in blood exposure and/or dislocation of the needle.

FDAJul 11, 2005Nationwide• Becton Dickinson & Company

Tubside Bath Seats (Safety 1st) – Child Safety Concern (2005)

These Safety 1st Tubside Bath Seats have model number 44301 engraved on the bottom of the base. "Safety 1st" is printed on the front of the units. They are white and blue, have a swivel seat and an elbow cushion on the attachment arm. These seats are intended for use with children from 5 months to 10 months of age.

CPSCJul 6, 2005Nationwide• Dorel Juvenile Group, of Columbus, Ind.

Becton Dickinson Medical Systems: DT-DL60-1 W/Bifurcated

Device could permit an over-infusion of IV solutions during pressure monitoring procedures.

FDAJul 1, 2005Nationwide• Becton Dickinson Medical Systems

Exercise Bench (Nautilus) – Structural Weakness (2005)

The Nautilus NT 1020 is a free-standing exercise bench typically used for free weight workouts. It is comprised of a white steel base with wheels on one end, with a black vinyl bench and back support. The fronts of both the white base and the black vinyl back support are stamped with the name "Nautilus." A tag affixed to the reverse side of the back support includes "Distributed by Nautilus/Schwinn Fitness Group Inc." and "Made in China." At the bottom of the product's base, near its wheels, is a sticker that includes the words "Production Date Code" and a 4-digit number. The first three digits of the date code identify the day and the fourth digit identifies the year in which the unit was built. Units included in this recall have Production Date Codes from year 2002 that run between code numbers 1952 and 3652, and Production Date Codes from year 2003 that run between code numbers 0013 and 1903. Benches that are white in color and do not have a Production Date Code sticker also are included in this recall.

CPSCJul 1, 2005Nationwide• Daytona Fitness Co., of Xiamen, China

Becton Dickinson Medical Systems: TAKHPQ60R continuous flow catheter.

Device could permit an over-infusion of IV solutions during pressure monitoring procedures.

FDAJul 1, 2005Nationwide• Becton Dickinson Medical Systems

Becton Dickinson Medical Systems: CRITIFLOW(tm) TA4004 continuous flush catheter

Device could permit an over-infusion of IV solutions during pressure monitoring procedures.

FDAJul 1, 2005Nationwide• Becton Dickinson Medical Systems

Becton Dickinson Medical Systems: BD DTX Plus, 12'' single-line neonatal pressure monitorin...

Actuating tab may detach from the stopcock body, allowing fluid leak.

FDAJul 1, 2005Nationwide• Becton Dickinson Medical Systems