95,018 total recalls in our database
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
units manufactured in a limited time period may emit electromagnetic noise beyond the acceptable limits for RTCA application specified in RTCA DO-160G Chapter 21, Equipment Category M.
Intuitive Surgical
Robotic-assisted surgical system has Viewer Display manufactured with outdated firmware, may result in loss of one display-loss of 3D surgical field (depth perception) but 2D maintained, or loss of both displays-complete visualization loss, without fault, instruments remain active, could lead to instrument contact with tissue, resulting in injury/bleeding; may require alternate surgical modality.
Medline Industries
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
AVID Medical
Tyvek bag seal issue which may compromise sterility of the kit.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
Philips North America
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
Due a design issue where the navigated array connection geometry is incorrect.
The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
Diva Fam
potential Clostridium botulinum contamination
Undeclared allergens (milk, soy, and peanut)
Tai Phat Wholesalers
Undeclared sulfites
Diva Fam
potential Clostridium botulinum contamination
potential Clostridium botulinum contamination
Undeclared allergens: egg and milk
potential Clostridium botulinum contamination