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Medtronic Gastroenterology Urology

Medtronic Gastroenterology Urology Recalls

All product recalls associated with Medtronic Gastroenterology Urology.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 36421–36440 of 37661 recalls

Medtronic Gastroenterology Urology: Bravo pH Monitoring System Receiver

The product's rear panel label could smear during use causing the serial number to be unreadible. This has the remote possibility of resulting in patient data from diagnostic tests being mixed-up or attributed to the wrong patient.

FDAFeb 6, 2004Nationwide• Medtronic Gastroenterology Urology

General Electric Med Systems: Seneographe 2000D Digital Mammography X-Ray System

The mammography system's information for users lacked the technical specification for the minimum filtration permanently installed in the useful beam and the technical specification for the maximum line current.

FDAFeb 6, 2004Nationwide• General Electric Med Systems

General Electric Med Systems: Seneographe 800T Mammography X-Ray Systems

1...1820 182118221823 1824...1884

Page 1822 of 1884Next

FDAFeb 6, 2004Nationwide• General Electric Med Systems

General Electric Med Systems: Seneographe 600 Mammography X-Ray Systems (all versions)

FDAFeb 6, 2004Nationwide• General Electric Med Systems

Varian Medical Systems: EPROM and Control Software (embedded), version 5.08, for ...

Radiation treatment software could potentially cause a healthcare practitioner to apply incorrect treatment regimen to patients undergoing brachytherapy.

FDAFeb 6, 2004Nationwide• Varian Medical Systems

General Electric Med Systems: Seneographe 700T Mammography X-Ray Systems

FDAFeb 6, 2004Nationwide• General Electric Med Systems

Becton Dickinson Infusion Therapy: BD Introsyte-N Precision Introducer in 1.9Fr. Bulk, Non-s...

Splittable catheter introducer may not fully split or may separate non-uniformly.

FDAFeb 3, 2004Nationwide• Becton Dickinson Infusion Therapy

Datex-Ohmeda Inc One Ohmeda: Datex-Ohmeda S/5 and AS/3 Anesthesia Delivery Units (...

Anesthetic agents could be delivered at concentrations above the concentration set on the S/5 and AS/3 Anesthesia Delivery Units (ADU) having serial numbers within a specified range.

FDAFeb 3, 2004Nationwide• Datex-Ohmeda Inc One Ohmeda

Becton Dickinson Infusion Therapy: BD First PICC Introsyte-N, 1.9Fr. x 50cm Single Lumen Pr...

Splittable catheter introducer may not fully split or may separate non-uniformly.

FDAFeb 3, 2004Nationwide• Becton Dickinson Infusion Therapy

Fuji Power Batteries (Dorcy) – Battery Defect (2004)

Fire/Burn Risk

Each of the 3-volt lithium batteries has a white label with the words "Fuji Power" or "A&T Fuji Power CR123A." The batteries were provided separately in pairs in packaging with the flashlights.

CPSCFeb 3, 2004Nationwide• Dorcy International Inc. of Columbus, Ohio

Action Products Incorporated: Xact(tm) Drop Seat Base, a plastic seat support in Xact (...

Wheelchair seat may not properly support the user due to cracks in the plastic seat base.

FDAFeb 2, 2004Nationwide• Action Products Incorporated

Richard Wolf Medical Instruments Corp.: Pump Tube, REF 8170,121; Suction Pump Drain Tube; An acce...

If the drain tube is assembled incorrectly, the suction pump will not operate as intended.

FDAFeb 2, 2004NE, TX• Richard Wolf Medical Instruments Corp.

NERF Big Play Football (Hasbro) – Design Flaw (2004)

Laceration Risk

The NERF® Big Play Football™ is a red and silver NERF football with a silver flip-open top that reveals an erasable writing pad to plan football plays on, in the center of the ball. The NERF name, an NFL logo and a large black "X" are on the silver region of the football. Mike Vick's signature in red also is written on the football, and his photo is on the packaging.

CPSCJan 30, 2004Nationwide• Hasbro Inc., of Pawtucket, R.I.

Medtronic Xomed, Inc.: The product is a sheath meant to fit over a Nasopharyngos...

The sheaths in question have shafts that are one inch longer than required for the endoscope specified on the label.

FDAJan 29, 2004FL, ID, IN +12 more• Medtronic Xomed, Inc.

Medtronic Xomed, Inc.: Product is a surgical nasal/sinus surgical device labeled...

The curve in the shaft of the bur was only 15 degrees not the labeled 40 degrees.

FDAJan 29, 2004FL, ID, IN +12 more• Medtronic Xomed, Inc.

Medtronic Xomed, Inc.: Product is a device used in adenoid surgery and is labele...

The box label indicates that the product is a size 2 whereas a size 4 was packed inside.

FDAJan 29, 2004FL, ID, IN +12 more• Medtronic Xomed, Inc.

Medtronic MiniMed: Medtronic MiniMed Model 7311 Version 5.0B Solutions Pumps...

A minor software anomaly results in an error in the calculation of the average glucose range that appears on one of the reports available in the model 7311 software.

FDAJan 28, 2004Nationwide• Medtronic MiniMed

Boston Scientific Corporation: Wallstent Rx Biliary Endoprosthesis with Unistep Plus Del...

Incorrect label states stent covered with 'Permalume Covering', product is uncovered

FDAJan 28, 2004CA, GA, MD +4 more• Boston Scientific Corporation

Beckman Coulter Inc: IgG Antisera component of the paragon Electrophoresis IF...

Inconsistent and incomplete results for IgG.

FDAJan 28, 2004Nationwide• Beckman Coulter Inc

System 2 Pool Filters (Sta-Rite) – Performance Issue (2004)

These modular pool filters are designed for use with above ground pools and small in-ground pools. These filters are used to remove particles from the water. The System 2 product line is sold under the brand names "Sta-Rite" and "AquaTools," located on a decal on the upper tank shell. The cylindrical filter tank measures 27 inches high and 18 inches in diameter. Sta-Rite System 2 filter tanks were sold with model numbers beginning with PLM or PLD and AquaTools filter tanks were sold with model numbers beginning with AT84100, AT84150 or AT82130. Serial numbers are located on on the nameplate decal on the upper tank shell. Only filters with the following serial numbers are affected (the 5th character is irrelevant for the purposes of this recall): 1A03_ 1B03_ 1C03_ 1D03_ 1EH03_ 1F03_ 1G03_ 1H03_ 1J03_ If the Posi-Lok™ locking ring has the phrase "Lubricate Tank "O" Ring - see instructions" molded into it, the ring has been updated and no further action is necessary for that filter.

CPSCJan 28, 2004Nationwide• Sta-Rite Industries, Inc. of Delavan, Wis.