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Displaying 1 - 15 of 321 items.
In case the magnets of the Novastar TS and Novastar Plus are positioned near medical devices (implanted as well as not-implanted) and metallic implants the magnetic field might impact the implants or devices and cause serious injury.
Recall start date…
RecallHealth product recall | 2023-01-24
Presence of particulate matter in affected lot.
RecallHealth product recall | 2023-01-18
Medline Industries, LP is recalling custom procedure packs containing medtronic non-absorbable sutures due to a manufacturing error in the packaging of the sutures that may cause a gap or wrinkle in the breather pouch seal resulting in a sterile barrier…
RecallHealth product recall | 2023-01-11
For certain nuclear medicine systems, GE Healthcare has become aware that a mitigation may not be correctly implemented. If this is the case, the detector can fall leading to life-threatening bodily injury.
Recall start date: December 18, 2022
RecallHealth product recall | 2022-12-30
The replacement silicone sound abatement foam installed into the Trilogy 100 and Trilogy 200 devices identified in this letter may separate from the plastic backing to which it is attached. If this were to happen, the foam could potentially block air…
RecallHealth product recall | 2022-12-21
Philips has identified an issue where a specific component failure in the gradient coil of where the affected 3T MR Systems identified above may act as a heat source, with a potential to produce smoke and/or fire.
If the components failure…
RecallHealth product recall | 2022-12-16
Affected lot may result in a false negative for skin test (peanut allergy).
RecallHealth product recall | 2022-12-14
Infolding is a known phenomenon and occurs when the valve frame folds inward along a vertical line away from the valve inflow and appears as a seam in the frame or as overlapping frame cells on radiographic imaging. Infolding is different and distinct…
RecallHealth product recall | 2022-12-13
Medtronic has determined that there were manufacturing errors in the packaging of the listed nonabsorbable sutures that may cause a gap or wrinkle in the breather pouch seal resulting in a sterile barrier breach. The potential harms of a sterile barrier…
RecallHealth product recall | 2022-12-13
Baxter Corporation is issuing an urgent medical device correction related to two different software issues that occur during use. The first issue observed is due to incorrect reported delivered volume while an infusion is running. The second issue…
RecallHealth product recall | 2022-12-09
Affected lot contains active ingredient (Cholecalciferol) levels outside of the labelled claim.
RecallHealth product recall | 2022-12-08
Teleflex has initiated a voluntary field safety corrective action due to a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices. These IABP devices can be powered either by connecting to an ac power source…
RecallHealth product recall | 2022-11-24
Affected lot may result in a false negative for skin test (peanut allergy)
RecallHealth product recall | 2022-11-15
Intravenous bag may be leaking in affected lots.
RecallHealth product recall | 2022-11-03
Affected lot is labelled with the incorrect strength and ingredient
RecallHealth product recall | 2022-10-24