8MM,MICRO BIPOLAR FORCEPS,IS4000 REF 471171
Intuitive Surgical
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
95,018 total recalls in our database
Intuitive Surgical
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Sklar Instruments
Reports of various packaging issues that may result in a breach of the sterile barrier.
Intuitive Surgical
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Intuitive Surgical
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Tornier S.A.S.
The Pin Guide is being recalled because the metal tube may disassemble from the plastic handle. This can result in the Blueprint Mixed Reality headset being unable to detect the Pin Guide and potentially prolonging surgery time or changing of surgical method from guided to conventional.
Intuitive Surgical
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Intuitive Surgical
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Intuitive Surgical
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Intuitive Surgical
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Intuitive Surgical
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Sklar Instruments
Reports of various packaging issues that may result in a breach of the sterile barrier.
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare has become aware that certain Infinia, VariCam/VG/VH, Brivo NM 615, Discovery NM 630, Discovery NM/CT 670, and Optima NM/CT 640 Nuclear Medicine systems (see Affected Products Details and Appendices) could have been transported or relocated without proper detector support, which can result in excessive load being applied to the detector mounting mechanisms. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.
A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built before September 2018, have an increased potential to initiate Safety Mode during telemetry or other normal, higher-power operations due to latent high battery impedance.
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare has become aware that certain Infinia, VariCam/VG/VH, Brivo NM 615, Discovery NM 630, Discovery NM/CT 670, and Optima NM/CT 640 Nuclear Medicine systems (see Affected Products Details and Appendices) could have been transported or relocated without proper detector support, which can result in excessive load being applied to the detector mounting mechanisms. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.
A possible sterility issue was detected in Coloplast's facility on some Coloplast products.
Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
Sklar Instruments
Reports of various packaging issues that may result in a breach of the sterile barrier.
Augustine Temperature Management
HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".