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Bodum + Starbucks Recycled Coffee Press recalled due to a laceration risk

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/69702r-eng.php

May 2, 2019 ... Summary Product: Bodum + Starbucks Recycled Coffee Press Issue: Coffee press' plunger knob may break and expose the metal rod inside, posing a laceration risk. What to do: Immediately stop using this product and contact Starbucks for a store credit. Affected products What you should do Joint recall with Health Canada, the United States Consumer Product Safety

Asena GH and Alaris Syringe Pumps (2018-06-25)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/67188r-eng.php

Jul 5, 2018 ... Pump (Rebranding) Reason While the pump is infusing, a breakage of the plunger backplate spring may allow movement of the syringe plunger that may result in siphonage. Neonatal and Pediatric patients, or those receiving critical drugs at low infusion rates, would be considered to be the most at risk if small volumes of fluids reach the patient due to siphoning

Cobas e801 Syringes (2018-03-23)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/66520r-eng.php

Apr 24, 2018 ...-66520 Reason Affected products Affected products Cobas e801 Syringes Reason The plunger of the Cobas e801 syringe assembly may be mounted in a tilted position which applies mechanical stress to the plunger and may cause r1, r2 or prewash liquids to be pipetted incorrectly. Affected products Cobas e801 Syringes Lot or serial number 1601-01 To 18E6-10 Model

FACSLyric Instrument - FACS Universal Loading Option (2018-04-30)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/66972r-eng.php

Jun 6, 2018 ..., Hospitals Identification number: RA-66972 Reason Affected products Affected products FACS UNIVERSAL LOADING OPTION Reason Incorrect solenoid length (plunger length too short) which resulted in insufficient engagement to the Universal Auto Loader (UAL) enclosure to lock during use. Affected products FACS UNIVERSAL LOADING OPTION Lot or serial number R651166000173

Alaris PCA and Syringe Module Models (2017-11-23)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/65352r-eng.php

Dec 8, 2017 ... Identification number: RA-65352 Reason Affected products Affected products A. ALARIS PCA MODULE MODEL 8120 B. ALARIS SYRINGE MODULE MODEL 8110 Reason The syringe plunger grippers may fail to automatically close around the syringe plunger press when the gripper control knob has been closed. It is important to note that the syringe plunger gripper can be manually closed

1 mL Medallion Syringe (2018-02-08)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/66254r-eng.php

Mar 23, 2018 ...: RA-66254 Reason Affected products Affected products 1 mL Medallion Syringe Reason Merit Medical Systems, Inc. are voluntarily conducting a recall of specific lots of 1 ml medallion syringes due to a supplier manufacturing defect with the syringe plunger tip. Prior to use and during prep, when fluid is drawn into the syringe, air may enter the barrel

Bradshaw Canada Holdings Inc. recalls Bialetti Coffee Press

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/63252r-eng.php

May 16, 2017 ... Joint recall with Health Canada, the United States Consumer Product Safety Commission (US CPSC) and Bradshaw Canada Holdings Inc. Affected products Bialetti Coffee Press Product description This recall involves Bialetti coffee presses with a glass beaker in a plastic frame with a stainless steel metal plunger. The coffee presses were sold in blue, green, black

Asena GH and Alaris Syringe Pumps (2017-05-04)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/63490r-eng.php

Jun 5, 2017 ... (Rebranding) Reason While the pump is infusing, a breakage of the plunger backplate spring may allow movement of the syringe plunger that may result in siphonage. Neonatal and paediatric patients, or those receiving critical drugs at low infusion rates, would be considered to be the most at risk if small volumes of fluids reach the patient due to siphoning. Affected

CS300, CS100 and CS100i Intra Aortic Balloon Pumps (2017-06-20)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2017/63968r-eng.php

Jul 17, 2017 ..., and an autofill failure, which has been associated to a patient death due to the failure of the device to initiate therapy. An electrical test failure code #58 is caused by a solenoid valve requiring more power than the solenoid driver board can deliver to open the valve. The lack of power prevents the coil from moving the plunger causing the valve not to open

60 cc Handy-Vak Locking Syring (November 03, 2005)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2005/10909r-eng.php

Mar 1, 2015 ..., Healthcare Professionals, Hospitals Identification number: RA-30621 Reason Affected products Reason Potential for the plunger to separate from the piston of the syringe. Affected products 60 cc Handy-Vak Locking Syringe Lot or serial number 39608 Model or catalog number MX 500 Companies Manufacturer Not Applicable Date modified: 2015-03-01

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