Manufacturer

Becton Dickinson & Company

179 recalls in our database name Becton Dickinson & Company as the manufacturing or recalling firm.

What the numbers show

Total: 179
Critical: 0
Severe: 22
Most recent: 2026-06-10

Of the 179 recalls from Becton Dickinson & Company we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 22 (12%) are Severe.

Which agencies issued them

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

76–100 of 179

ModerateFDA (Devices)·Z-0285-2020·2019-11-13
Becton Dickinson Recalls 13 Fr Trialysis Catheters Due to Packaging Error
Becton Dickinson is recalling 75 units of 13 Fr Trialysis Catheters because a portion of the lot was incorrectly packaged with a 12.5cm catheter instead of a 15cm catheter.
Product
13 Fr. Trialysis Catheter with Alphacurve. Catalog No. 5653150. UDI: 00801741066023 Power-Trialysis Short-Term Alphacurve Dialysis Catheter with a third internal umen for IV therapy, power injection of contrast media, and central venous pressure monitoring.
Category
Medical Device
Distribution
6 states
HighFDA (Devices)·Z-0252-2020·2019-11-06
BD Vacutainer Eclipse Blood Collection Needles Recalled for Missing Bevel
Becton Dickinson is recalling specific lots of BD Vacutainer Eclipse Blood Collection Needles because a missing bevel on the non-patient end caused blood leakage.
Product
BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-0193-2020·2019-10-30
BD Vacutainer Push Button Blood Collection Set Recalled for Barrel Separation
Becton Dickinson is recalling 1.7 million BD Vacutainer Push Button Blood Collection Sets because the front and rear barrels may separate when the needle retracts.
Product
BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This product is designed to provide customers an increased level of safety during IV blood collection, convenience and to improve OSHA single-use holder compliance. F
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0049-2020·2019-10-16
Becton Dickinson Recalls CareFusion MaxPlus Clear Needleless Connectors
Becton Dickinson is recalling 115,200 CareFusion MaxPlus Clear Needleless Connectors because the valve may fail to close, posing risks of blood loss and air embolism.
Product
CareFusion MaxPlus Clear Needleless Connector. Intended for Positive Displacement Connector for needleless access to the IV line and/or IV catheter during IV therapy Cat. No. MP1000-C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0055-2020·2019-10-16
BD Microtainer Tubes Recalled for Damaged Reservoirs and Erroneous Test Results
Becton Dickinson is recalling specific lots of BD Microtainer Tubes with Lithium Heparin because damaged reservoirs may cause insufficient sample volumes and erroneous test results.
Product
BD Microtainer Tubes with LH (Lithium Heparin) Part/Catalog No.365965
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0056-2020·2019-10-16
Becton Dickinson Recalls BD Microtainer SST Tubes Due to Damaged Reservoirs
Becton Dickinson is recalling BD Microtainer SST tubes because damaged reservoirs may cause insufficient sample volume and erroneous test results.
Product
BD Microtainer SST Part/Catalog No.365967
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0054-2020·2019-10-16
Becton Dickinson Recalls BD Microtainer Z Tubes Due to Damaged Reservoirs
Becton Dickinson & Company is recalling BD Microtainer Z No Additive Tubes because damaged reservoirs may cause insufficient sample volumes and erroneous test results.
Product
BD Microtainer Z (No Additive Tubes) Part/Catalog No.365963
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0059-2020·2019-10-16
BD Microtainer PSTTubes with Lithium Heparin Recalled for Damaged Reservoirs
Becton Dickinson & Company is recalling BD Microtainer PSTTubes with Lithium Heparin because damaged reservoirs may cause insufficient sample volumes and erroneous test results.
Product
BD Microtainer PSTTubes with LH (Lithium Heparin) Part/Catalog Number:365985
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0057-2020·2019-10-16
BD Microtainer Tubes Recalled for Damaged Reservoirs Causing Test Errors
Becton Dickinson is recalling BD Microtainer Tubes with K2E because damaged reservoirs may cause insufficient sample volume and erroneous test results.
Product
BD MicrotainerTubes with K2E (K2EDTA) Catalog Number: 365974
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0060-2020·2019-10-16
BD Microtainer PST Tubes Recalled for Damaged Reservoirs
Becton Dickinson is recalling BD Microtainer PST Tubes with Lithium Heparin because damaged reservoirs may cause insufficient sample volume and erroneous test results.
Product
BD Microtainer PST Tubewith LH (Lithium Heparin) - Amber Part/Catalog Number: 365987
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0061-2020·2019-10-16
BD Microtainer Tubes Recalled Due to Damaged Reservoirs
Becton Dickinson is recalling specific lots of BD Microtainer Tubes with FE Glycolytic Inhibitor because damaged reservoirs may cause insufficient sample volumes and erroneous test results.
Product
BD Microtainer Tubes with FE (Sodium Fluoride / Disodium EDTA) Glycolytic Inhibitor Part/Catalog Number: 365992
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0058-2020·2019-10-16
BD Microtainer SST- Amber Tubes Recalled for Damaged Reservoirs
Becton Dickinson is recalling specific lots of BD Microtainer SST- Amber tubes because damaged reservoirs may cause insufficient sample volumes and erroneous test results.
Product
BD Microtainer SST- Amber Part/Catalog Number: 365978
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2411-2019·2019-09-04
Becton Dickinson Recalls Jamshidi Bone Marrow Biopsy Needles Due to Sterility Concerns
Becton Dickinson is recalling 700 units of Jamshidi Crown Bone Marrow biopsy needles because product pouches may not be sealed properly, potentially compromising sterility.
Product
8 G x 10 CM Jamshidi Crown Bone Marrow biopsy/Aspiration Needle with MAC Catalog Number: TMJ4008
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-2301-2019·2019-08-28
BD Vacutainer Tubes Recalled for False Carboxyhemoglobin Results
Becton Dickinson is recalling specific blood collection tubes because they may cause falsely elevated carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Product
BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 367960
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2296-2019·2019-08-28
BD Vacutainer Tubes Recalled for False Carboxyhemoglobin Results
Becton Dickinson is recalling BD Vacutainer Lithium Heparin blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.
Product
BD Vacutainer Lithium HeparinN (LH) 37 USP Units Blood Collection Tubes, Catalog Number 366664
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2297-2019·2019-08-28
BD Vacutainer Lithium Heparin Tubes Recalled for False COHb Results
Becton Dickinson is recalling BD Vacutainer Lithium Heparin blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.
Product
BD Vacutainer Lithium HeparinN (LH) 56 USP Units Blood Collection Tubes, Catalog Number 366667
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2303-2019·2019-08-28
BD Vacutainer Tubes Recalled for False Carboxyhemoglobin Results
Becton Dickinson is recalling specific blood collection tubes because they may cause falsely elevated carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Product
BD Vacutainer PST Gel and Lithium HeparinN (LH) 83 Units Blood Collection Tubes, Catalog Number 367962
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2306-2019·2019-08-28
BD Vacutainer Tubes Recalled for False Carboxyhemoglobin Results
Becton Dickinson is recalling BD Vacutainer PST Blood Collection Tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Product
BD Vacutainer PST Blood Collection Tubes, Catalog Number 368035, 368036
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2298-2019·2019-08-28
BD Vacutainer Lithium Heparin Tubes Recalled for False COHb Results
Becton Dickinson is recalling BD Vacutainer Lithium Heparin blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.
Product
BD Vacutainer Lithium HeparinN (LH) 158 USP Units Blood Collection Tubes, Catalog Number 367880
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2304-2019·2019-08-28
BD Vacutainer Blood Collection Tubes Recalled for False COHb Results
Becton Dickinson is recalling specific blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Product
BD Vacutainer PST Gel and Lithium HeparinN (LH) Blood Collection Tubes, Catalog Number 367963
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2308-2019·2019-08-28
BD Vacutainer Blood Collection Tubes Recalled for False COHb Results
Becton Dickinson is recalling BD Vacutainer LH blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.
Product
BD Vacutainer LH (Lithium Heparin) 34 I.U. Plus Blood Collection Tubes, Catalog Number 368494
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2305-2019·2019-08-28
BD Vacutainer Blood Collection Tubes Recalled for False COHb Results
Becton Dickinson is recalling specific blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Product
BD Vacutainer PST Gel and Lithium HeparinN (LH) 126 Units Blood Collection Tubes, Catalog Number 367964
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2307-2019·2019-08-28
BD Vacutainer Blood Collection Tubes Recalled for False COHb Results
Becton Dickinson is recalling BD Vacutainer PST Gel and Lithium Heparin blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Product
BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 368056
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2310-2019·2019-08-28
BD Vacutainer Lithium Heparin Tubes Recalled for False COHb Results
Becton Dickinson is recalling BD Vacutainer LH blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Product
BD Vacutainer LH (Lithium Heparin) 102 I.U. Plus Blood Collection Tubes, Catalog Number 368886
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2300-2019·2019-08-28
BD Vacutainer Tubes Recalled for False Carboxyhemoglobin Results
Becton Dickinson is recalling BD Vacutainer Lithium Heparin blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.
Product
BD Vacutainer Lithium HeparinN (LH) 95 USP Units Blood Collection Tubes, Catalog Number 367886
Category
Medical Device
Distribution
Distributed nationwide