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Becton Dickinson & Recalls
364 recalls on record · July 25, 2012 to June 10, 2026 · Drugs, Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
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The recall feeds record what looks like the same company under more than one name:
May 27, 2020Medical DevicesFDA
Becton Dickinson & Company recalls BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000277
Hazard: The kits contain surgical gowns which were subject to a recall by the supplier.
May 27, 2020Medical DevicesFDA
Becton Dickinson & Company recalls BARD MYPICC KIT 4F Single-Lumen, Catalog Number CK000276
Hazard: The kits contain surgical gowns which were subject to a recall by the supplier.
May 27, 2020Medical DevicesFDA
Becton Dickinson & Company recalls BARD MYPICC KIT 5F Triple-Lumen, Catalog Number CK000026A
Hazard: The kits contain surgical gowns which were subject to a recall by the supplier.
May 27, 2020Medical DevicesFDA
Becton Dickinson & Company recalls BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000025
Hazard: The kits contain surgical gowns which were subject to a recall by the supplier.
May 27, 2020Medical DevicesFDA
Becton Dickinson & Company recalls BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535
Hazard: This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.
May 27, 2020Medical DevicesFDA
Becton Dickinson & Co. recalls BD BBLTM Gram Stain Kit with Stabilized Iodine-- IVD For the differential staining of bacteria, Catalog Number: 212539 -
Hazard: May exhibit increased levels of artifacts which could be difficult to distinguish from gram positive cocci, increased levels of artifacts could result in a false-positive Gram stain
May 27, 2020Medical DevicesFDA
Becton Dickinson & Co. recalls BD BBLTM Gram Crystal Violet 3.8L-- IVD Primary stain for Staining Microorganisms, Catalog Number: 212526 - Product Usag
Hazard: May exhibit increased levels of artifacts which could be difficult to distinguish from gram positive cocci, increased levels of artifacts could result in a false-positive Gram stain
May 27, 2020Medical DevicesFDA
Becton Dickinson & Co. recalls BD BBLTM Gram Crystal Violet 250mL-- IVD Primary stain for Staining Microorganisms, Catalog Number: 212525 - Product Usa
Hazard: May exhibit increased levels of artifacts which could be difficult to distinguish from gram positive cocci, increased levels of artifacts could result in a false-positive Gram stain
May 20, 2020Medical DevicesFDA
Becton Dickinson & Company recalls PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
Hazard: Iincorrectly packaged without the required lidocaine as labeled
May 6, 2020Medical DevicesFDA
Becton Dickinson & Company recalls CareFusion Safe-T-Centesis Catheter Drainage Tray, Sterile, For Single Use Only, Rx only, Catalog Number PIG1280T, UDI N
Hazard: The 8 Fr catheter was manufactured with the 6.9 Fr needle instead of the 8 Fr needle.
December 4, 2019Medical DevicesFDA
Becton Dickinson & Company recalls Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound imaging of the human body. Site~Rite 8 Ultrasound Sys
Hazard: The indicator may show available charge when the battery is close to depletion. As a result, the Site~Rite 8 has the potential to abruptly shut down, without advance warning to the user, when running on battery power only
November 27, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575 (Canada only)
Hazard: Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.
November 27, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547
Hazard: Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.
November 13, 2019Medical DevicesFDA
Becton Dickinson & Company recalls 13 Fr. Trialysis Catheter with Alphacurve. Catalog No. 5653150. UDI: 00801741066023 Power-Trialysis Short-Term Alphac
Hazard: A portion of the lot was incorrectly packaged with a 12.5cm catheter instead of a 15cm catheter.
November 13, 2019Medical DevicesFDA
Becton Dickinson & Company recalls MaxZero Extension Sets with Needle-less Connector, Product codes MZ1000 MZ1000-07 MZ5301 MZ5302 MZ5303 MZ5304 M
Hazard: BD has decided to initiate a voluntary recall due to a confirmed complaint trend for droplets of fluid separating from the sealed surface of the MaxZero connector, following disconnection.
November 6, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
Hazard: BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage.
October 30, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This p
Hazard: Separation of front and rear barrels upon activation of the safety feature that retracts the needle
October 16, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Microtainer Tubes with FE (Sodium Fluoride / Disodium EDTA) Glycolytic Inhibitor Part/Catalog Number: 365992
Hazard: Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.
October 16, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Microtainer PST Tubewith LH (Lithium Heparin) - Amber Part/Catalog Number: 365987
Hazard: Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.
October 16, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Microtainer PSTTubes with LH (Lithium Heparin) Part/Catalog Number:365985
Hazard: Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.
October 16, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Microtainer SST- Amber Part/Catalog Number: 365978
Hazard: Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.
October 16, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD MicrotainerTubes with K2E (K2EDTA) Catalog Number: 365974
Hazard: Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.
October 16, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Microtainer SST Part/Catalog No.365967
Hazard: Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.
October 16, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Microtainer Tubes with LH (Lithium Heparin) Part/Catalog No.365965
Hazard: Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.
October 16, 2019Medical DevicesFDA
Becton Dickinson & Company recalls BD Microtainer Z (No Additive Tubes) Part/Catalog No.365963
Hazard: Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.
October 16, 2019Medical DevicesFDA
Becton Dickinson & Company recalls CareFusion MaxPlus Clear Needleless Connector. Intended for Positive Displacement Connector for needleless access to the
Hazard: After disconnection of a luer, the valve of the connector remains recessed; not fully closing, either temporarily or permanently. The risks of blood loss and air embolism exist if the valve remains permanently open and goes undetected, especially in the neonate population.
September 11, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls BD Kiestra InoqulA+ Software Version 20.3. IVD automated specimen processing Catalog Number : 447213
Hazard: An anomaly is present in InoqulA / InoqulA+ software version 20.3, has the potential to cause a mismatch between a specimen and plate
September 11, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls BD Kiestra InoqulA Software Version 20.3.IVD automated specimen processing Catalog Number: 447202
Hazard: An anomaly is present in InoqulA / InoqulA+ software version 20.3, has the potential to cause a mismatch between a specimen and plate
September 4, 2019Medical DevicesFDA
Becton Dickinson & Company recalls 8 G x 10 CM Jamshidi Crown Bone Marrow biopsy/Aspiration Needle with MAC Catalog Number: TMJ4008
Hazard: Product Pouches may not be sealed properly and compromise the sterility of the device
August 28, 2019Medical DevicesFDA
Becton Dickinson & Co. recalls Kit BD Max Enteric Viral Panel EU Catalog # 443985
Hazard: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.