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Recall Observatory FDA recall evidence

Device product

Pedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringe Rx Only Genesis BPS, LLC The intended use is to prepare and deliver small aliquots of filtered whole blood, red blood cells, platelets, plasma, and cryoprecipitate for pediatric and or neonatal transfusion.

Z-2669-2014

July 17, 2014

Class II

Product summary

Firm
Genesis BPS, LLC.
Event
Event 68874
Status
Terminated
Classification
Class II
Quantity
4608 units
Official record key
device-enforcement:Z-2669-2014

Official wording

Reason: Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.

Code information: Cat #405-535MJ Lot # 3650-23970; 3650-24518; 3650-23477; 3650-23507; 3650-24331; 3650-24396; 3650-24486; 3650-25301

Distribution pattern: Nationwide Distribution & Switzerland

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.