Becton, Dickinson And Company
17200 Laguna Canyon Rd, Irvine, CA, US
Registered product codes
35 product codes
Recent MDR events
20,906 on file
- BD Vacutainer® Eclipse¿ Signal¿ Blood Collection Needle with Integrated HolderJul 30, 2026Malfunction9617032-2026-01297
- BD Vacutainer® Eclipse¿ Signal¿ Blood Collection Needle with Integrated HolderJul 30, 2026Malfunction9617032-2026-01298
- BD Vacutainer® 9NC 0.109M Plus Blood Collection TubesJul 29, 2026Malfunction9617032-2026-01275
- BD Vacutainer® SST¿ II Advance Plus Blood Collection TubesJul 29, 2026Malfunction9617032-2026-01282
- BD Vacutainer® SST¿ II AdvanceJul 29, 2026Malfunction9617032-2026-01286
- BD Vacutainer® SST¿ II AdvanceJul 29, 2026Malfunction9617032-2026-01287
- BD Vacutainer® Eclipse¿ Signal¿ Blood Collection Needle with Integrated HolderJul 29, 2026Malfunction9617032-2026-01283
- BD Vacutainer® Eclipse¿ Signal¿ Blood Collection Needle with Integrated HolderJul 29, 2026Malfunction9617032-2026-01285
- BD Vacutainer® Eclipse¿ Signal¿ Blood Collection Needle with Integrated HolderJul 29, 2026Malfunction9617032-2026-01284
- BD Vacutainer® 9NC 0.109M Plus Blood Collection TubesJul 29, 2026Malfunction9617032-2026-01280
Recalls
73 on file
- Open, ClassifiedMay 15, 2026
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
View FDA record ↗ - Open, ClassifiedMay 15, 2026
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
View FDA record ↗ - Open, ClassifiedMay 15, 2026
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
View FDA record ↗ - Open, ClassifiedAug 1, 2025
Control kits contain incorrect standard deviation (SD) values for the low and high control beads which compromises the accurate calculation of bead counts.
View FDA record ↗ - Open, ClassifiedAug 1, 2025
Control kits contain incorrect standard deviation (SD) values for the low and high control beads which compromises the accurate calculation of bead counts.
View FDA record ↗ - Open, ClassifiedJul 3, 2025
Due to customer complaints, errors in spectral overlap factors table for 7-color setup beads may affect accurate setup of the flow cytometry instrument prior to analyzing samples.
View FDA record ↗ - Open, ClassifiedJul 3, 2025
Due to customer complaints, errors in spectral overlap factors table for 7-color setup beads may affect accurate setup of the flow cytometry instrument prior to analyzing samples.
View FDA record ↗ - Open, ClassifiedDec 23, 2024
On October 18, 2024, BD has identified through customer complaints and an increase in field failures / replacements of the power supply module (part number 650781, Power Module AC-DC 250W 12/24V M3S4S6) on BD FACSLyric flow cytometers, which has the potential for the instruments to fail to power on and/or stay on. The potential power supply failure on BD FACSLyric Flow Cytometer may lead to risks to the laboratory staff including inhalation of fumes followed by shortness of breath or coughing if failure occurs during laboratory working hours. The patient may be asked to return for additional biospecimen collection procedure and risks associated with the procedure (bruising, pain, bleeding, etc.). In addition, patient specimen loss and/ or delay providing results of testing results. There may be additional risks to the laboratory staff including inhalation of fumes followed by shortness of breath or coughing if failure occurs during laboratory working hours. In addition, the patient may be asked to return for additional biospecimen collection procedure and risks associated with the procedure (bruising, pain, bleeding, etc.). In the Notification Letter sent on November 20, 2024, customers are instructed to continue their normal operation of your BD FACSLyric Flow Cytometer according to the Instructions For Use after immediately inspecting inventory for the specific catalog and power supply serial numbers listed in the notification letter and follow the instructions listed under Actions for Clinical Users
View FDA record ↗ - Open, ClassifiedDec 23, 2024
On October 18, 2024, BD has identified through customer complaints and an increase in field failures / replacements of the power supply module (part number 650781, Power Module AC-DC 250W 12/24V M3S4S6) on BD FACSLyric flow cytometers, which has the potential for the instruments to fail to power on and/or stay on. The potential power supply failure on BD FACSLyric Flow Cytometer may lead to risks to the laboratory staff including inhalation of fumes followed by shortness of breath or coughing if failure occurs during laboratory working hours. The patient may be asked to return for additional biospecimen collection procedure and risks associated with the procedure (bruising, pain, bleeding, etc.). In addition, patient specimen loss and/ or delay providing results of testing results. There may be additional risks to the laboratory staff including inhalation of fumes followed by shortness of breath or coughing if failure occurs during laboratory working hours. In addition, the patient may be asked to return for additional biospecimen collection procedure and risks associated with the procedure (bruising, pain, bleeding, etc.). In the Notification Letter sent on November 20, 2024, customers are instructed to continue their normal operation of your BD FACSLyric Flow Cytometer according to the Instructions For Use after immediately inspecting inventory for the specific catalog and power supply serial numbers listed in the notification letter and follow the instructions listed under Actions for Clinical Users.
View FDA record ↗ - Open, ClassifiedDec 23, 2024
On October 18, 2024, BD has identified through customer complaints and an increase in field failures / replacements of the power supply module (part number 650781, Power Module AC-DC 250W 12/24V M3S4S6) on BD FACSLyric flow cytometers, which has the potential for the instruments to fail to power on and/or stay on. The potential power supply failure on BD FACSLyric Flow Cytometer may lead to risks to the laboratory staff including inhalation of fumes followed by shortness of breath or coughing if failure occurs during laboratory working hours. The patient may be asked to return for additional biospecimen collection procedure and risks associated with the procedure (bruising, pain, bleeding, etc.). In addition, patient specimen loss and/ or delay providing results of testing results. There may be additional risks to the laboratory staff including inhalation of fumes followed by shortness of breath or coughing if failure occurs during laboratory working hours. In addition, the patient may be asked to return for additional biospecimen collection procedure and risks associated with the procedure (bruising, pain, bleeding, etc.). In the Notification Letter sent on November 20, 2024, customers are instructed to continue their normal operation of your BD FACSLyric Flow Cytometer according to the Instructions For Use after immediately inspecting inventory for the specific catalog and power supply serial numbers listed in the notification letter and follow the instructions listed under Actions for Clinical Users.
View FDA record ↗
Compliance history
Matched by FEI 3032916632.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.