Recall notifications

For questions pertaining to a specific medical device recall, please see the contact information within the product recall notice or customer letter.

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Recall notification - BD FACSTM Sample Prep Assistant II and III

Jul 8, 2019

BD FACSTM Sample Prep Assistant II and III

Recall notification - Alaris EtCO2 Module model 8300

Jul 3, 2019

BD has identified an issue with the AlarisEtCCh Module Model 8300 that is detected duringdevice implementation.

Recall notification - BD Accuri C6 Plus

Jun 13, 2019

This recall notification is for BD Accuri C6 Plus

Recall notification - BD Vacutainer® Fluoride Tubes for Blood Alcohol Determinations

Jun 12, 2019

BD Vacutainer® Fluoride Tubes for Blood Alcohol Determinations

Recall notification - BD Vacutainer® Plastic Lithium Heparin Tubes

Jun 12, 2019

This recall notification is for BD Vacutainer® Plastic Lithium Heparin Tubes

Recall notification - Difco Biotin Assay Medium

Jun 11, 2019

This recall notification is for Difco Biotin Assay Medium

Recall notification - BD Microtainer® Tubes w/ BD MicrogardTM Closure, K2EDTA additive

Jun 3, 2019

This recall notification is for BD Microtainer® Tubes w/ BD MicrogardTM Closure, K2EDTA additive

Recall notification - BD Microtainer® Tubes

May 13, 2019

This recall notification is for BD Microtainer® Tubes

Recall notification - Alaris Pump Infusion Sets

May 6, 2019

This recall notification is for Alaris Pump Infusion Sets

Recall notification - MaxPlus Clear Needleless Connector

May 2, 2019

This recall notification is for MaxPlus Clear Needleless Connector

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