There is a potential performance issue as detected by an under-recovery of sample results during routine testing.
Other Medical Devices
🏥 Medical Devices • 15,809 recalls
INTEGRA, Drill CS 4.5, quick coupling single use, REF 430453
AAP Implantate Ag
Products were distributed with the incorrect instructions for use.
INTEGRA, Drill CS 4.0, quick coupling single use, REF 430425
AAP Implantate Ag
Products were distributed with the incorrect instructions for use.
Urine Electrolyte Diluent, Product Code: 1112352 - Product Usage: used to dilute urine specimens for analysis of sodium (Na+) and potassium (K+) on VITROS 250/350/5,1 FS/4600 Chemistry Systems and the VITROS 5600/XT 7600 Integrated Systems.
Ortho Clinical Diagnostics
Potential for the instability of the diluents VITROS 7% BSA (Product Code 8262487) and VITROS Urine Electrolyte Diluent (UED) (Product Code 1110352) when stored in a 2mL cup for 7 days.
Lamicel 20PK 3MM INTL Cervical dilator
Medtronic Xomed
Routine sterilization dose does not meet the required Sterility Assurance Level.
Potential for the instability of the diluents VITROS 7% BSA (Product Code 8262487) and VITROS Urine Electrolyte Diluent (UED) (Product Code 1110352) when stored in a 2mL cup for 7 days
Certain Aespire and Aestiva Anesthesia Systems were noted to have a vulnerability to a cyber-attack when connected to the hospital network. An insufficiently secured terminal server may provide an opportunity for a malicious actor that has already penetrated the hospital network to send fraudulent flow sensor correction parameters.
A1CNow SELF CHECK (European), Software Version Revision D, REF Numbers 3054, 3062
Polymer Technology Systems
A numerical value less than 4% or greater than 13% may be displayed instead of the expected <4% or >13% result, due to a software bug.
There is a potential patient health risk while performing chronic hemodialysis treatments in the home setting with for patients with low blood volume (2.4 Liters or less in a patient with body weight of 30kg or less) when prescribing larger dialysate volumes.
A limited number of lenses may be mislabeled with the incorrect diopter power.
Artis zee/ zeego Interventional Fluoroscopic X-Ray System, Model Number: 10094142, Software Version: VC21C
Siemens Medical Solutions USA
In affected Artis zee floor Interventional Fluoroscopic X-Ray Systems, the activation of a collision sensor will cause a block the movement of the floating tabletop and could result in a delay or interruption of a procedure.
A1CNow+ Systems (professional use product), Software Version Revision D, REF Numbers US: 3021, 3024; EU: 3037, 3038, 3057, 3058
Polymer Technology Systems
A numerical value less than 4% or greater than 13% may be displayed instead of the expected <4% or >13% result, due to a software bug.
QuickTox 5 Panel Drug Screen DipCard
Ameditech
Mixed Products containing QuickTox 5 Panel Drugs Screen Dipcard (P/N QT11, LOT #188787) and Alere iScreen Drugs of Abuse Dip Test (P/N X11-IS10-22015-DX LOT #188744)
Under certain circumstances, the percutaneous pin adapter used with the StealthAir Frame Assembly may slightly rotate after surgical placement and not return to its original position, even when connections are tight and secure.
Rhondium OVC3 One Visit Crown, Model FDI 24/25L USA 12/13L A2 HT, Nonsterile, Rx. The firm name on the label is Rhondium Ltd., Katikati, New Zealand.
RHONDIUM LIMITED
The product was mislabeled with an incorrect expiration date.
Medtronic Affinity, 38um Arterial Filter, Catalog number REF 351
Medtronic Perfusion Systems
Medtronic has identified an out of-specification condition exhibiting excess plastic (flash) in the arterial filter directly above the outlet port.
Elasto-Gel Absorbent Wound Dressing, Item DR8000. 5 Dressings 4" x 4". Sterile. UPC 45713-58000 Bacteriostatic
Southwest Technologies
Elasto-Gel Wound Dressing may be contaminated with mold.
Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A
Medline Industries
The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit.
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
Integra LifeSciences
The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not meet the Dry Time Criteria for a 30-minute drying cycle. The current CUSA Clarity Operators manual states 30 minutes for the minimum Dry Time for the 36 kHz Sterilization Tray and 36 kHz Components but 40 minutes is required for complete drying.
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
Integra LifeSciences
The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not meet the Dry Time Criteria for a 30-minute drying cycle. The current CUSA Clarity Operators manual states 30 minutes for the minimum Dry Time for the 36 kHz Sterilization Tray and 36 kHz Components but 40 minutes is required for complete drying.