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Symbia T series Gamma Camera/CT Scanners (2019-07-11)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/70523r-eng.php

Jul 26, 2019 ...Symbia T series Gamma Camera/CT Scanners (2019-07-11) Report a Concern Starting date: July 11, 2019 Posting date: July 26, 2019 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type II Source of recall: Health Canada Issue: Medical Devices Audience: General Public, Hospitals Identification number: RA-70523 Last

AIRO Mobile CT Scanner (2018-08-07)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/67458r-eng.php

Aug 17, 2018 ...AIRO Mobile CT Scanner (2018-08-07) Report a Concern Starting date: August 7, 2018 Posting date: August 17, 2018 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type I Source of recall: Health Canada Issue: Medical Devices Audience: General Public, Healthcare Professionals, Hospitals Identification number: RA

Revolution CT - Main Unit, Revolution CT ES (2019-06-06)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/70267r-eng.php

Jun 21, 2019 ... Identification number: RA-70267 Last updated: 2019-06-21 Reason Affected products Affected Products A. Revolution CT - Main Unit B. Revolution CT ES Reason GE Healthcare has become aware of two potential issues on Revolution CT Scanners that could cause additional low dose radiation exposure. Affected products A. Revolution CT - Main Unit Lot or serial number More than

Optima CT540 Series CT Scanner System (2018-04-27)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/67276r-eng.php

Jul 19, 2018 ...Optima CT540 Series CT Scanner System (2018-04-27) Report a Concern Starting date: April 27, 2018 Posting date: July 19, 2018 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type II Source of recall: Health Canada Issue: Medical Devices Audience: General Public, Healthcare Professionals, Hospitals

AIRO Mobile CT Scanner (2017-09-26)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/64788r-eng.php

Oct 6, 2017 ...AIRO Mobile CT Scanner (2017-09-26) Report a Concern Starting date: September 26, 2017 Posting date: October 6, 2017 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type II Source of recall: Health Canada Issue: Medical Devices Audience: Hospitals, Healthcare Professionals, General Public Identification number

Somatom Emotion 16-Slice Configuration and Somatom Perspective - CT Scanner (2018-02-05)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/66124r-eng.php

Mar 13, 2018 ...Somatom Emotion 16-Slice Configuration and Somatom Perspective - CT Scanner (2018-02-05) Report a Concern Starting date: February 5, 2018 Posting date: March 13, 2018 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type II Source of recall: Health Canada Issue: Medical Devices Audience: General Public

Symbia T series Gamma Camera/CT Scanners, Symbia Intevo and Symbia Intevo Bold (2018-05-16)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/66986r-eng.php

Jun 6, 2018 ...Symbia T series Gamma Camera/CT Scanners, Symbia Intevo and Symbia Intevo Bold (2018-05-16) Report a Concern Starting date: May 16, 2018 Posting date: June 6, 2018 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type II Source of recall: Health Canada Issue: Medical Devices Audience: General Public, Healthcare

LOGIQ P6 Ultrasound System - Main Unit and LOGIQ P6 Ultrasound System - Console Upgrade to BT09 (2018-12-27)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/68852r-eng.php

Jan 23, 2019 ... these scanners with specific probes. This could result in a burn to the patient in specific types of scans. Affected products A. LOGIQ P6 Ultrasound System - Main Unit Lot or serial number More than 10 numbers, contact manufacturer. Model or catalog number H46082LW Companies Manufacturer GE Ultrasound Korea Ltd. 9 Sunhwan-ro 214beon-gil Jungwon-gu. Seongnam, Gyeonggi 462

RTVUE OCT SCANNER (2016-04-18)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2016/58528r-eng.php

May 20, 2016 ...RTVUE OCT SCANNER (2016-04-18) Report a Concern Starting date: April 18, 2016 Posting date: May 20, 2016 Type of communication: Medical Device Recall Subcategory: Medical Device Hazard classification: Type III Source of recall: Health Canada Issue: Medical Devices Audience: General Public, Healthcare Professionals, Hospitals Identification number: RA-58528

ARIES and ARIES M1 System (2018-07-02)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/67228r-eng.php

Sep 4, 2018 ...-67228 Reason Affected products Affected products ARIES System ARIES M1 System Reason A potential discrepancy in the firmware for a subset of ARIES System Barcode Scanners (CN-0321-01). When the potentially affected barcode scanner is used on multiple ARIES Cassettes at the same time, the system may prepopulate the "sample id" field with a previously stored

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