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Vacuette® sample transfer unit

Official notice

7 Jan 2025

Last checked

7 Jan 2025

Medium riskHealth Canada

An official Health Canada notice concerns Vacuette® sample transfer unit. Reports to Greiner indicate several lots of the sample transfer units (stu) may leak due to the protective rubber sleeve bunching up and not retracting when using the device. The non reset of the rubber sleeve can depend on the device age and can be up to 23%. The sample transfer unit (stu) is a custom-made, single-use tube holder, used solely in plasma centers, to transfer a small amount of plasma from the bottle to the tube. Once transferred in the tube, plasma samples are tested to assure quality standards/specifications of the bottled plasma are met prior to sale. No patient treatment is performed at plasma centers. Since there is no venous pressure and personal protective equipment (PPE) is required when handling plasma samples, the risk to the user is minimal. Any possible leakage does not impact the device's capability to collect plasma sample nor the quality of the plasma sample. As a result, the potential effects of the detected error are viewed as low risk. Nevertheless, the leakage could still pose a minimal risk to the user, specifically if appropriate PPE is not worn. Therefore, the concerned lots of the device should not be utilized. Recall start date: November 4, 2024 Published 2025-01-07.

What to do now

Contact the manufacturer if you require additional information.

Recall number

76802

Official notice

2025-01-07

The hazard

Reports to Greiner indicate several lots of the sample transfer units (stu) may leak due to the protective rubber sleeve bunching up and not retracting when using the device. The non reset of the rubber sleeve can depend on the device age and can be up to 23%. The sample transfer unit (stu) is a custom-made, single-use tube holder, used solely in plasma centers, to transfer a small amount of plasma from the bottle to the tube. Once transferred in the tube, plasma samples are tested to assure quality standards/specifications of the bottled plasma are met prior to sale. No patient treatment is performed at plasma centers. Since there is no venous pressure and personal protective equipment (PPE) is required when handling plasma samples, the risk to the user is minimal. Any possible leakage does not impact the device's capability to collect plasma sample nor the quality of the plasma sample. As a result, the potential effects of the detected error are viewed as low risk. Nevertheless, the leakage could still pose a minimal risk to the user, specifically if appropriate PPE is not worn. Therefore, the concerned lots of the device should not be utilized. Recall start date: November 4, 2024

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Recall Numbers

76802

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Affected products

Product 1

Affected products - VACUETTE® Sample Transfer Unit, Lot or serial number - B240749R B2407379 B24083NM B24083AK B240837T B24063KJ, Model or catalog number - 450218

Risk / hazard

Reports to Greiner indicate several lots of the sample transfer units (stu) may leak due to the protective rubber sleeve bunching up and not retracting when using the device. The non reset of the rubber sleeve can depend on the device age and can be up to 23%. The sample transfer unit (stu) is a custom-made, single-use tube holder, used solely in plasma centers, to transfer a small amount of plasma from the bottle to the tube. Once transferred in the tube, plasma samples are tested to assure quality standards/specifications of the bottled plasma are met prior to sale. No patient treatment is performed at plasma centers. Since there is no venous pressure and personal protective equipment (PPE) is required when handling plasma samples, the risk to the user is minimal. Any possible leakage does not impact the device's capability to collect plasma sample nor the quality of the plasma sample. As a result, the potential effects of the detected error are viewed as low risk. Nevertheless, the leakage could still pose a minimal risk to the user, specifically if appropriate PPE is not worn. Therefore, the concerned lots of the device should not be utilized. Recall start date: November 4, 2024

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: REI, Vacuette® Sample Transfer Unit.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

76802

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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