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Nokia BPM+ (2018-12-17)

Jan 23, 2019 ... Reason Affected products Affected products Nokia BPM+ Reason BPM+ is an upper arm blood pressure monitor that measures systolic and diastolic pressure, and heart rate. It is intended to be used at home by an adult with an arm circumference ranging from 22 to 42 cm. It was identified that the device was less accurate on subjects with larger arm circumference


Mar 17, 2016 ..., Hospitals Identification number: RA-57564 Reason Affected products Affected Products A. TASK FORCE MONITOR Reason The monitors showed a non-conformity in the production process which may lead to incorrect measurement values of the oscillometric (upper arm) blood pressure measurement. Affected products A. TASK FORCE MONITOR Lot or serial number More than 10 numbers

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Mar 30, 2012 ... (Monday-Friday). Please note that the Canada Consumer... Posted: 2019-01-18 Type of communication: Recall Sonolith i-sys System (2019-01-17) Sonolith i-sys System (2019-01-17) Affected Products Sonolith i-sys System In case of rupture of the monitor arm fixing element, the system tilts laterally on a height of about 500 mm but remains retained to its support

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Mar 30, 2012 ..., hormone replacement therapy) may be at an elevated... Posted: 2014-05-23 Type of communication: Advisory Hypertension drug PMS-Losartan-HCTZ recalled due to labelling error PMS-Losartan-HCTZ 100/25mg is a combination product of both losartan (100 mg) and hydrochlorothiazide (HCTZ, 25mg) used for the treatment of hypertension (high blood pressure). One lot is being

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Mar 30, 2012 ... of the blister card in the Cautions and Warnings section where the word "not" was omitted giving the following erroneous information: "It is recommended to use this product with natural health products, ephedra, other drugs that increase blood pressure or other caffeine-containing... Posted: 2012-03-28 Type of communication: Recall Undeclared egg and chemical additives

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Mar 30, 2012 ...) Recalled Products Maryland DissectorSingle Site Crocodile GrasperSingle Site Medium - Large Clip ApplierSingle-set Needle Driver Under rare circumstances, grip-actuated instruments may become fixed in a closed position. ,,, A. Maryland Dissector, B. Single... Posted: 2015-08-25 Type of communication: Recall CDI BLOOD PARAMETER MONITORING SYSTEM 500 - MONITOR

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Mar 30, 2012 ... Canada Inc. This is duplicated text of a letter from Pfizer Canada Inc. Contact the company for a copy of any references,... Posted: 2005-06-30 Type of communication: Advisory Archived – Reminder: Canadian Requirements for White Blood Cell Monitoring for Patients Taking Clozaril* Archived – Reminder: Canadian Requirements for White Blood Cell Monitoring

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Mar 30, 2012 ... events using this product to Health Canada. Contact Alive Health Centre at 1-604-263-3235 to return the product. Health Canada is monitoring the recall of Alive Vitamins - Royal Jelly 1200 mg by Alive... Posted: 2014-01-03 Type of communication: Advisory Sublinox (zolpidem tartrate) - New Dosage Recommendations to Minimize Risk of Next-Day Impairment in Both

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Mar 30, 2012 ....... Posted: 2016-02-18 Type of communication: Recall MACK issued a recall on the GU, and MRU models MACK issued a recall on the GU, and MRU models On certain vehicles, the roll pin may not have been installed on the upper yoke on the steering shaft during assembly. If the roll pin is missing, the steering shaft may disconnect from the yoke. Separation of the shaft

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Mar 30, 2012 ... (2016-07-08) ULTRAVIEW SL COMMAND MODULE (2016-07-08) Affected products A. ULTRAVIEW SL COMMAND MODULE Spacelabs has received multiple reports of the Non-invasive Blood Pressure (NIBP) parameter becoming non-functional with an associated message (no reading). In addition, there is one of the following three error... Posted: 2016-07-08 Type of communication

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