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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=11000&plain_text=&s=

Mar 30, 2012 ... are recalled the CFIA will notify the public through updated Food Recall Warnings.The CFIA... Posted: 2014-02-26 Type of communication: Recall Hintegra Tibial and Talar Implants and Revision Components (2014-02-25) Hintegra Tibial and Talar Implants and Revision Components (2014-02-25) Recalled Products A. Hintegra Tibial Implant B. Hintegra Talar Implant with Pegs C

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=0&plain_text=&s=

Mar 30, 2012 ... Products Atellica CH Reaction Cuvette Segment Siemens Healthcare Diagnostics has determined that a small percentage (... Posted: 2020-02-17 Type of communication: Recall BladderScan BVI 3000 (2020-02-14) BladderScan BVI 3000 (2020-02-14) Affected Products BladderScan BVI 3000 The BVI 3000 has a feature that enables display of the User Set Date on the device's

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=2000&plain_text=&s=

Mar 30, 2012 .... To their knowledge this... Posted: 2018-08-15 Type of communication: Recall Various B.Braun Medical Inc's Catheter Connector, Nerve Block Sets, Epidural Catheter Sets, Epidural Catheter Tray and Epidural Sets (2018-08-14) Various B.Braun Medical Inc's Catheter Connector, Nerve Block Sets, Epidural Catheter Sets, Epidural Catheter Tray and Epidural Sets (2018-08-14) Affected

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=3000&plain_text=&s=

Mar 30, 2012 ... for the child. For more information, consumers may contact Shermag Inc. at 1-800-567-3419, from Monday to Friday... Posted: 2017-12-12 Type of communication: Recall Peg Perego Canada Inc. recalls Various Book Strollers Consumers should immediately stop using the recalled strollers and contact Peg Perego Canada Inc. or register on their website to receive a retrofit kit

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Mar 30, 2012 ...Search interface for Health Canada website

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https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/search-recherche/simple?js_en=&page=1000&per_page=14000&plain_text=&s=

Mar 30, 2012 ...: Recall Depth Gauge 6 - 65 mm (November 20, 2012) There are two scales laser marked on the 6-65 mm depth gauge and they are different from each other by 2 mm. Adequate fixation may not be obtained because the screw selected may be shorter than desired. 138525 1 251896 80-0623 Depth Gauge 6 - 65 mm (2012-11-20) 2015-03-01 16:56:51 2015-03-01... Posted: 2012-11-20

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Mar 30, 2012 ...... Posted: 2006-08-29 Type of communication: Recall Continu-Flo Sets with Check Valv (August 29, 2006) Baxter is providing information regarding the use of this device with a secondary infusion, potential for solutions from the secondary container to pass the check valve and enter backflow into primary container. 111833 1 All lot numbers JC0430, JC5380N, JC5381N

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Mar 30, 2012 ... Monitor B. Infinity Delta XL Patient Monitor Draeger was informed about a case in which the affected units running VF10.0 software did not generate a set low O2 alarm although the O2 level that was measured by the... Posted: 2017-03-31 Type of communication: Recall Wilson Frame Pad Wilson Frame Pad An audit of the manufacturing process has discovered a variance

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Mar 30, 2012 ...,... Posted: 2016-09-10 Type of communication: Advisory LIFEPAK 15 MONITOR/DEFIBRILLATOR LIFEPAK 15 MONITOR/DEFIBRILLATOR Affected Products Physio-Control, Inc. LIFEPAK 15 Monitor/Defibrillators with End-tidal(Et)CO2 capability are distributed with the EtCO2 setting preset to display in (millimeter of mercury) mmHg. Customers may choose to reconfigure the device

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Mar 30, 2012 ... THE BRAKE STOPLAMP SWITCH CONTACTS MAY EITHER NOT CLOSE OR NOT OPEN RESULTING IN TWO POSSIBLE SETS OF CONDITIONS. FIRST, IF THE SWITCH CONTACTS WILL NOT CLOSE, THE BRAKE STOPLAMPS WILL NOT ILLUMINATE AND THE... Posted: 1990-01-01 Type of communication: Recall GENERAL MOTORS issued a recall on the S SERIES model GENERAL MOTORS issued a recall on the S SERIES model

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