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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

620

Class I (Serious)

91

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 10081–10100 of 10937 recalls

Disetronic Medical Systems, Inc.: Accu-Chek Ultraflex soft DUS 1 infusion set; 8 mm (60 cm)...

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.

Disetronic Medical Systems, Inc.: Accu-Chek Ultraflex 1-infusion set; 8 mm 24'' (60 cm); Ca...

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.

Disetronic Medical Systems, Inc.: Accu-Chek FlexLink 1 infusion set; 8/30; Ref number 04540...

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

1...503 504505506 507...547

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

Disetronic Medical Systems, Inc.: Accu-Chek FlexLink Cannula 8; Ref number 04541219001. (D...

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.

Disetronic Medical Systems, Inc.: Accu-Chek FlexLink Cannula 10; Ref number 04541227001. (...

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.

Disetronic Medical Systems, Inc.: Disetronic Ultraflex 10/110 infusion set; (Distributed o...

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.

Disetronic Medical Systems, Inc.: Disetronic Ultraflex 8/60 infusion set; (Distributed out...

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.

Disetronic Medical Systems, Inc.: Disetronic Ultraflex 8/110 infusion set; (Distributed ou...

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.

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.

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.

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

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)

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

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.

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

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