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Phantom® Hindfoot TTC/TC Ball Tipped Guide Rod
Sterility
La Vera Group Pty Ltd- La Vera Cheddar Pepper R/W approx 300g
Food Recall Alert
Greenworks Tools Recalls 24V and 48V Kobalt Yard Power Tools with USB-C Batterie...
Charging the lithium-ion batteries through the USB-C port, while the batteries are inserted in the yard power tools can cause the batteries to short-circuit, posing a risk of serious injury from fire hazard.
ºM Warmer
Performance
Moodooy Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapmen...
The recalled bed rails violate the mandatory standard for?adult portable bed rails?because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation.?In addition, the bed rails do not bear the required hazard warning labels.
Biometric Gun Safes Recalled Due to Serious Injury Hazard and Risk of Death; Sol...
The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.
eliquid france - diy citron vert arôme concentré eliquid france
problème d’étiquetage : absence des mentions suivantes :¤danger : liquide et vapeurs très inflammable ¤tenir à l’écart de la chaleur....¤contient : limonène, citral. peut produire une réaction allergique¤+ pictogramme flamme et triangle tactile
bmw - série 1 (e81 e82 e87 e88) - série 3 (e90 e91 e92 e93) voiture partic...
le propulseur dans l'airbag du conducteur peut se détériorer avec le temps. si les airbags se déploient, des fragments du gonfleur pourraient blesser les occupants du véhicule.
Conair Recalls Cuisinart Propel+ Four Burner 3-In-1 Gas Grills Due to Risk of Se...
The tempered glass window in the pizza oven can shatter during use, posing a risk of serious injury from laceration hazard.
bmw - série 1 (e82, e88) voiture particulière
le propulseur dans l'airbag du conducteur peut se détériorer avec le temps. si les airbags se déploient, des fragments du gonfleur pourraient blesser les occupants du véhicule.
ARTIS icono biplane. Model Number: 11327600.
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator...
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control pendant, the collimator may release and fall from the housing.
Medline Convenience Kits: 1) ARTERIAL LINE KIT, Model Number: ART890B; 2) ULT...
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
Medline Convenience Kits: 1) OPHTHALMIC PACK W/LIDO, Model Number: DYNJ57922A
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
Medtronic Harmony Delivery Catheter System
Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system under certain procedural or anatomical conditions due to a manufacturing issue.
Medline Convenience Kits: 1) MERCY MEDICAL CIRCUMCISION TRAY, Model Number: CIT...
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
ARTIS icono ceiling. Model Number: 11328100.
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
Radius VSM Disposable NIBP Cuff, REF: 4825, 4826
Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate patients, which may distract clinicians away from management of true positive alarms, which could delay treatment; 2) Small and medium size blood pressure cuffs may contain rough edges, may result in skin irritation/redness.
CRE Wireguided 15-18mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401...
Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection. If particulate were to dislodge during use and contact circulating blood or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.
Medline Convenience Kits: 1) BLOCK TRAY, Model Number: DYNJRA1590
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.
A M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgical...
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
CRE Pro Wireguided 8-10mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen...
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.