Class I - Dangerous
Reports of the infusion tubing disconnecting from the connector, resulting in leakage of insulin from the infusion set and providing patient with less insulin than intended.
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Infusion Pumps
🏥 Medical Devices • 4,262 recalls
Class I - Dangerous
Reports of the infusion tubing disconnecting from the connector, resulting in leakage of insulin from the infusion set and providing patient with less insulin than intended.
Class I - Dangerous
Stryker Medical has identified a potential issue associated with Secure II and S3 Med/Surg beds built between April 2nd, 2005 and July 26th, 2011. The affected beds have the potential to experience damage to the Foot End Cover and/or Power Coil Cable due to reduced clearance between the Foot End Cover and Foot End Lift Header.
Class I - Dangerous
Stryker Medical has identified a potential issue associated with Secure II and S3 Med/Surg beds built between April 2nd, 2005 and July 26th, 2011. The affected beds have the potential to experience damage to the Foot End Cover and/or Power Coil Cable due to reduced clearance between the Foot End Cover and Foot End Lift Header.
Class I - Dangerous
Reports of the infusion tubing disconnecting from the connector, resulting in leakage of insulin from the infusion set and providing patient with less insulin than intended.
X-ray system C-arm casting may loosen and fall
Class I - Dangerous
Reports of the infusion tubing disconnecting from the connector, resulting in leakage of insulin from the infusion set and providing patient with less insulin than intended.
Class I - Dangerous
Reports of the infusion tubing disconnecting from the connector, resulting in leakage of insulin from the infusion set and providing patient with less insulin than intended.
Class I - Dangerous
Screw inserters may not mate properly with hex interface of the screws.
Class I - Dangerous
Screw inserters may not mate properly with hex interface of the screws.
Class I - Dangerous
Screw inserters may not mate properly with hex interface of the screws.
McKesson Radiology 12.0, Picture Archiving Communication System (PACSA).
Mckesson Information Solutions
Class I - Dangerous
When merging two patient records into one patient record using McKesson Radiology 12.0, the resulting patient record is missing the Contrast Allergy information for the second patient record.
Class I - Dangerous
Promotional materials for non-medical water filtration products were determined to promote claims which constitute marketing the product as a medical device.
Qualigen initiated this recall because the FastPack kit may cause lower than expected results due to a manufacturing defect.
Promotional materials for non-medical water filtration products were determined to promote claims which constitute marketing the product as a medical device.
Qualigen initiated this recall because the FastPack kit may cause lower than expected results due to a manufacturing defect.
Qualigen initiated this recall because the FastPack kit may cause lower than expected results due to a manufacturing defect.
Promotional materials for non-medical water filtration products were determined to promote claims which constitute marketing the product as a medical device.
Baxter Healthcare Corporation is issuing a voluntary correction for ABACUS Total parenteral Nutrition (TPN) Calculation Software versions 2.0 through 3.0 due to the possibility that a patient could receive another patient's TPN order as a result of data corruption.
Maquet has received an increase in the number of complaints for "self-activated/remains activated/overheats" for the Hemopro VH-30000, "Hemopro 1"