🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
All Recalls
95,075 total recalls in our database
🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
Quantum Intersegmental Table, Model/Catalog Number: Q400; heated massage table
Pivotal Health Solutions
🏥 Medical Devices Class I - Dangerous
The heat function may become damaged over time due to patients pressing on the areas with heat function components. Damage to components can lead to overheating which can lead to smoldering and melting of the vinyl cushion.
🏥 Medical Devices Class I - Dangerous
The IFU (Information for Use) on the wrap instructs the user to heat the hot and cold compression wrap in the microwave for 3 minutes, which may cause the wrap to leak or break at the seams and/or reach temperatures capable of causing a second degree burn.
🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
🏥 Medical Devices Class I - Dangerous
Continued reports of positive cultures and infections have identified updates to the reprocessing materials to minimize potential deviations in TJF duodenoscope reprocessing. Olympus is informing users of these changes, reminding users to closely follow the operation and reprocessing instructions, and providing updated materials to users.
🏥 Medical Devices Class I - Dangerous
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
SJM Pericardial Patch, with EnCap Technology 9x14cm, Model Number REF C0914; PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE
Glycar SA Pty.
🏥 Medical Devices Class I - Dangerous
The impacted lot may not meet the required tensile strength specification.
FlexLab (FLX); Version: FLX-217-40;
Inpeco S.A.
🏥 Medical Devices Class I - Dangerous
The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results, this error occurs if the operators open the printer head of mALX to perform error recoveries or maintenance procedures and do not empty the printer tubes buffer to remove all the secondary sample tubes