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Disetronic Medical Systems, Inc.

Disetronic Medical Systems, Inc. Recalls

All product recalls associated with Disetronic Medical Systems, Inc..

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Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

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 16381–16400 of 17592 recalls

Disetronic Medical Systems, Inc.: Accu-Chek Ultraflex-10 infusion set; Catalog number 45447...

The luer tube may break at the lock-tubing connection to the pump, causing an interruption of insulin delivery, which can and has contributed to hyperglycemia

FDAMar 31, 2006Nationwide• Disetronic Medical Systems, Inc.

Beckman Coulter Inc: SYNCHRON Systems Vancomycin Reagent, in vitro diagnostic....

Beckman Coulter has received reports of patient samples and quality control recovery shifting low when using Vancomycin reagent lots M507219 and M511327. Internal QC recovery was as much as 15% lower than the assigned target value.

FDAMar 30, 2006Nationwide• Beckman Coulter Inc

American Girl Children's Jewelry – Lead Poisoning (2006)

The recall includes American Girl necklaces, bracelets, earrings and hair accessories for girls. The recall does not include jewelry for American Girl dolls. The jewelry's packaging features a red and white cardboard backing with "American Girl" and "Made in China" written on the front.

1...818 819820821 822...880

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CPSCMar 30, 2006Nationwide• American Girl Inc., of Middleton, Wis., a division of Mattel Inc., of El Segundo, Calif.

Smiths Medical MD, Inc.: Locator-Wand Cover that is sold in a shelf carton (unit ...

One lot of Locator-Wand Cover sterile pouches may have an insufficient seal and product sterility could be compromised. The Locator-Wand Cover is supplied with the PORT-A-CATH II AND P.A.S. PORT systems. The packaged Wand-Cover is placed on the outside of the PORT-A-CATH II AND P.A.S. PORT tray.

FDAMar 29, 2006Nationwide• Smiths Medical MD, Inc.

Delphi Medical Systems: Delphi IVantage Volumetric Ambulatory Infusion Pump/Syste...

Potential for under-infusion without alarm; cassette rollers stop moving , but the pump shaft continues rotating without alarm.

FDAMar 29, 2006FL• Delphi Medical Systems

Biological and Environmental Control Laboratories Inc: Aspergillus Niger Microbial Suspension, Model Numbers: 1...

Aspergillus niger microbial suspension, found to be contaminated with yeast, was distributed.

FDAMar 29, 2006CA, CO, GA +6 more• Biological and Environmental Control Laboratories Inc

GE OEC Medical Systems, Inc: MiniView 6800 Digital Mobile C-arm fluoroscopic x-ray sys...

Radiation exposure rate could exceed specifications during fluoroscopic x-ray procedure.

FDAMar 28, 2006Nationwide• GE OEC Medical Systems, Inc

Conmed Corporation: ConMed DetachaTip Multi-Use Laparoscopic Instrument - "Fe...

Grasper jaws breaking at the junction of the jaw and tube during laparoscopic procedures.

FDAMar 27, 2006Nationwide• Conmed Corporation

Fischer Imaging Corporation: SenoScan Full Field Digital Mammography System--Product N...

Software upgrade to preclude lost images during mammography procedure.

FDAMar 27, 2006Nationwide• Fischer Imaging Corporation

Valsi Portable Generators – Fire Hazard (2006)

Fire/Burn Risk

The Valsi "G" model G38MG0750RV, G42MG0750RV, G55MG0900RV, and G65MG1100RV are portable generators with black plastic fuel tank, full lifting frame, and side control panel. The recalled generators are black with blue label and have "Valsi Generator" printed on the label.

CPSCMar 22, 2006Nationwide• Corporativo Valsi S.A de C.V, Guadalajara, Mexico

Medtronic Emergency Response Systems, Inc.: LIFEPAK 20 defibrillator/monitor

Therapy connectors may have connector sockets that do not meet design specs - short drill depth. Interruption of the connections may cause unexpected, intermittent or complete loss of pacing and defibrillation functions.

FDAMar 22, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK 12 defibrillator/monitor

FDAMar 22, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Fresenius Medical Care North America: Newton IQ 4 Lead Cycler Set with stay-safe patient connec...

Stay safe trigger body may not connect to the extension set and result in associated peritonitis

FDAMar 22, 2006Nationwide• Fresenius Medical Care North America

Excelsior Medical Corp: ESP 140 Syringe Pump. Used for medication infusion. Mod...

Potential for alarm failure when the 140 pump completes infusion and/or the pump encounters a mid-infusion occlusion, when used in the 140 mode with a 140cc syringe. The ESP Pump works correctly when used in 60 mode with a 60cc syringe or smaller.

FDAMar 21, 2006Nationwide• Excelsior Medical Corp

Hitachi Medical Systems America Inc: MRP-7000, AIRIS Magnetic Resonance Imaging Systems

Software anomaly. A software defect in the referenced systems can cause a slice indicator (reference line) to be mis-positioned on the cross-reference image when it is magnified. This image error could result in a possible patient mis-diagnosis.

FDAMar 17, 2006Nationwide• Hitachi Medical Systems America Inc

Plasma Flat Panel TVs (Philips) – Potential Defect (2006)

The recall involves only certain 42- and 50-inch, 2005 model Philips branded Plasma Flat Panel Televisions with Ambilight technology, which is an ambient lighting feature that projects a soft light onto the wall behind the TV to enhance the display. They were manufactured with the following model, date codes, and serial numbers: Model Display Type Production Began Production Ended Beginning Serial Range Ending Serial Range 42PF9630A/37 Plasma April 2005 July 2005 AG1A0518xxxxxx AG1A0528xxxxxx 50PF9630A/37 Plasma May 2005 August 2005 AG1A0519xxxxxx AG1A0533xxxxxx 50PF9630A/37 Plasma June 2005 August 2005 YA1A0523xxxxxx YA1A0534xxxxxx 50PF9830A/37 Plasma June 2005 August 2005 AG1A0526xxxxxx AG1A0533xxxxxx The model and serial numbers can be found on the back of the TV on the label that looks like the example in the picture: The serial number can also be obtained by pushing the following keystrokes on the remote control: 123654, after which a customer service menu ("CSM") will be displayed on the screen. In the menu, line 03 displays the type number and line 04 displays the production code (identical to the serial number of the set). Press the MENU button on the remote to exit the CSM.

CPSCMar 16, 2006Nationwide• Philips Consumer Electronics North America, of Atlanta, Ga.

Medtronic Emergency Response Systems, Inc.: LIFEPAK 20 automatic external defibrillator

LIFEPAK 20 may lock-up when attempting to power-up on DC within 2 seconds after removing AC power.

FDAMar 16, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

B & K Medical Systems, Inc.: Convex Array Transducer used with B-K Ultrasound Scanners...

Due to a problem with calibration, the device can produce up to 50% elevated acoustic output and up to 2 degrees higher surface temperature

FDAMar 16, 2006CA, CT, FL +10 more• B & K Medical Systems, Inc.

Beckman Coulter Inc: Unicel DxC 600/800 SYNCHRON Clinical Systems; Operating S...

It was confirmed that the ORDAC (Over Range Detection And Correction) feature (auto & manual) does not perform correctly for the glucose cup chemistry (GLUCm) when sample type of 'Other' is selected w/operating software versions 1.0 & 1.2. Results for these samples could be elevated as much as twice the actual value. The ORDAC feature does function properly w/serum, plasma, urine & CSF.

FDAMar 15, 2006Nationwide• Beckman Coulter Inc

Beckman Coulter Inc: SYNCHRON LX 20, SYNCHRON LX 20 PROClinical Systems; Opera...

It was confirmed that the ORDAC (Over Range Detection And Correction) feature (auto & manual) does not perform correctly for the glucose cup chemistry (GLUCm) when sample type of 'Other' is selected w/operating software version 4.5. Results for these samples could be elevated as much as twice the actual value. The ORDAC feature does function properly w/serum, plasma, urine & CSF.

FDAMar 15, 2006Nationwide• Beckman Coulter Inc