Every recall we track for Becton Dickinson & Company — 137 in all — plus the complaints and injury reports the public filed about them.
Becton Dickinson recalls spinal trays with specific lidocaine and bupivacaine solutions due to quality issues found during FDA facility inspections. Affected units have catalog numbers 405671 and UDI numbers starting with (01)00382904056711.
Becton Dickinson recalls spinal trays with specific lidocaine and bupivacaine injections due to quality issues found during FDA facility inspections. Affected units have catalog numbers 400868 and 405652 with listed expiration dates.
Becton Dickinson recalls spinal trays with specific lidocaine and bupivacaine solutions due to quality issues found during FDA facility inspections. Affected units have catalog numbers 405609 and specific UDI numbers.
Becton Dickinson recalls spinal trays with specific lidocaine and bupivacaine injections due to quality issues found during FDA facility inspections. Affected units have catalog numbers 405658 and expiration dates up to October 2026.
Becton Dickinson recalls spinal trays and needles due to quality issues found during FDA facility inspections. This affects specific product models with catalog numbers 405741 and expiration dates up to October 2026.
Becton Dickinson recalls spinal trays with specific lidocaine and bupivacaine solutions due to quality deficiencies found during FDA facility inspections. Affected units have catalog numbers 405621 and 405735 with specific expiration dates.
Becton Dickinson recalls spinal trays with specific lidocaine and bupivacaine injections due to quality issues found during FDA facility inspections. Affected units have catalog numbers 400866-406704 with specific lot numbers.
Becton Dickinson recalls spinal trays with specific lidocaine and bupivacaine injections due to quality issues found during FDA facility inspections. Affected units have catalog numbers 405637 and 405707 with specific expiration dates.
Becton Dickinson recalls spinal trays with specific needle and anesthetic mixtures due to quality issues found during FDA facility inspections. Affected units have catalog numbers 405632 and UDI numbers starting with (01)00382904056322.
Becton Dickinson recalls spinal trays with specific lidocaine and bupivacaine solutions due to quality issues found during FDA facility inspections. Affected units have catalog numbers 405645 and expiration dates up to October 2026.
Becton Dickinson recalls 850 units of 10mL non-sterile Luer-Lok Tip Syringes (Catalog 301029) because some Luer Slip syringes were mistakenly included in the batch.
Becton Dickinson recalls Luer Tip Caps with catalog number 308341 due to failed biocompatibility testing. Affected units may pose health risks.
Becton Dickinson recalls 9 lots of 10mL PosiFlush Prefilled Saline Syringes with General Pump Compatibility due to incorrect stoppers causing increased injection force that may trigger syringe pump alarms.
BD recalls Alaris Pump infusion sets labeled as DEHP-free but actually contain di(2-ethylhexyl) phthalate (DEHP). Affected items have specific catalog numbers and were sold through medical suppliers. Contact BD for details.
Becton Dickinson recalls BD SmartSite Filter Extension Sets that contain di(2-ethylhexyl) phthalate (DEHP) instead of being DEHP-free. These sets may pose health risks during medical use.
Becton Dickinson recalls gravity sets that label themselves as DEHP-free but actually contain di(2-ethylhexyl) phthalate (DEHP). Affected sets have catalog numbers 4030B-07T and 42081E, sold through July 31, 2026.
Becton Dickinson recalls insulin syringes with Micro-Fine IV needle that may expose patients to infections due to nonsterile conditions. Affected units have specific catalog and lot numbers.
Becton Dickinson recalls 1mL insulin syringes (31G) due to potential nonsterile condition causing infections. Affected lots from 2045201 to 2073801 with expiration dates up to May 2027.
Becton Dickinson recalls 1mL insulin syringes (29G) due to potential nonsterile condition causing infections. Affected units include specific lot numbers and expiration dates.
Becton Dickinson recalls insulin syringes with nonsterile needles that may cause infections. Affected units have specific catalog and lot numbers. Consumers should check their syringes and contact the company for details.
Becton Dickinson recalls 0.5mL insulin syringes due to potential nonsterile condition risking infection. Affected units include specific lot numbers and expiration dates.
Becton Dickinson recalls BD Ultra-Fine Insulin Syringes (0.5mL, 6mm, 31G) due to potential nonsterile condition that could cause infections. Affected units have specific lot numbers and expiration dates.
Becton Dickinson recalls insulin syringes with nonsterile needles that may cause infections. Affected units have specific catalog and lot numbers. Consumers should check details and contact the company for remedies.
Becton Dickinson recalls BD Ultra-Fine Insulin Syringes (0.5mL, 8mm, 31G) due to nonsterile condition potentially causing infections. Affected lots expire by 2027.
Becton Dickinson recalls BD Vacutainer tubes with sodium fluoride (100mg) and potassium oxalate (20mg) due to potential false positive methanol test results in blood alcohol testing. All lots affected.
Becton Dickinson recalls BD PhaSeal Y-Site Connectors with incorrect expiration dates on labels. These devices may expire before use, risking medication safety. Affected units include specific lot numbers.
Becton Dickinson recalls BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (Catalog No. 394910) due to potential leakage causing treatment delays, exposure to biohazardous materials, and under-dosing risks. Affected units sold in the US from 2024.
Becton Dickinson recalls BD Connecta 3-Way Stopcocks (Catalog No. 394900) due to potential leakage that could delay treatment, cause contamination, or lead to under-dosing. Affected units sold from 2024 with specific lot numbers.
Becton Dickinson recalls BD Connecta Stopcock Without Extension Tube (Catalog No. 394605) due to potential leakage causing treatment delays, exposure to biohazardous materials, and under-dosing risks.
Becton Dickinson recalls BD Connecta Plus3 White Blend OEM (sterile, bulk) Catalog No. 395214 (OUS) due to potential leakage at the stopcock housing, which may cause treatment delays, contamination, or under-dosing.
Becton Dickinson recalls BD Connecta Plus1 360 Blue Blend infusion devices with catalog number 394911 (OUS) due to potential leakage at the stopcock housing, which could cause treatment delays, contamination, or under-dosing.
Becton Dickinson recalls Nexiva with Single BD Connecta Stopcock (20 Ga Blue) due to potential leakage causing treatment delays, exposure to biohazardous materials, and under-dosing. Affected units have specific catalog numbers and lot dates.
Becton Dickinson recalls BD Connecta Stopcock Without Extension Tube (Catalog No. 394602) due to potential leakage that could delay treatment, cause contamination, or lead to under-dosing. Affected units have specific lot numbers and expiration dates.
Becton Dickinson recalls BD Connecta White 360 Shelf 100Ea (Catalog No. 395000) due to potential leakage at the stopcock housing, which may cause treatment delays, contamination, or under-dosing. Affected units have specific lot numbers and expiration dates.
Becton Dickinson recalls pink Nexiva with Single BD Connecta Stopcock (Catalog 383687) due to potential leakage causing treatment delays, exposure to biohazardous materials, and under-dosing. Affected units sold between 2024-03-31 and 2024-07-31.
Becton Dickinson recalls BD Connecta Stopcock Without Extension Tube (Catalog No. 394600) due to potential leakage that could delay treatment, cause contamination, or lead to under-dosing. Affected units have specific lot numbers and expiration dates.
Becton Dickinson recalls BD Connecta Stopcock Without Extension Tube (Catalog No. 394601) due to potential leakage risks that could delay treatment, cause contamination, or lead to under-dosing. Affected units include specific lot numbers from March 2024 to April 2024.
Becton Dickinson recalls BD Vacutainer Luer Lok Access Devices that may shed contaminants into urine samples, leading to false high red blood cell counts when used with certain analyzers.
Becton Dickinson recalls BD Syringe Tip Cap Bulk Sterile Convenience Pak-1000 units due to packaging holes that may compromise sterility. Affected units have catalog number 305822 and lot number 1111347.
Becton Dickinson recalls 10ml eccentric tip syringes with open seals that could compromise sterility. Affected units have catalog number 305482 and expire May 2023. Consumers should check packaging for open seals.
Becton Dickinson recalls 50-unit packs of BD Stimex Insulated Needles (22G x 2.13in) due to outdated instructions for medication use. Affected units include specific catalog numbers and expiration dates.
Becton Dickinson recalls 50-unit packs of 22G regional block needles for updated safety instructions to prevent medication errors during anesthesia procedures.
Becton Dickinson recalls BD PrecisionGlide 30G needles with blood contamination risk. If blood is not noticed before use, infection may occur. Affected units: Lot 9128897, expired June 2024.
Becton Dickinson recalls BD Ultra-Fine Pen Needles 32G x 4mm (5/32') for missing US compatibility information in labeling. This affects users in the US who may not know if the needles work with their drug pens.
Becton Dickinson recalls Bard 3F SL PowerMidline Basic Kits that lack the stylet/T-lock assembly, potentially causing procedural delays or kit discards during IV therapy.
Becton Dickinson recalls Bard 3F SL PowerMidline Full Kits due to missing stylet/T-lock assembly, which could lead to procedural delays or kit discards during IV procedures.
Becton Dickinson recalls BD Nexiva Closed IV Catheter Systems with dull needles that could delay treatment. Learn if your product is affected and what to do.
Becton Dickinson recalls 50-unit packs of BD SafetyGlide 3mL syringes with incorrect scale markings that may lead to inaccurate dosing. Affected units have catalog # 305924 and lot # 8289599.
Becton Dickinson recalls SafeStep Huber Needle Sets with specific catalog numbers and lot numbers due to potential cracks in tubing that could cause leakage of chemotherapeutics or blood, leading to infection or other complications.
Becton Dickinson recalls PowerLoc MAX Power Injectable Infusion Sets with GuardIVa dressing due to potential tubing cracks causing chemical exposure or infection risks.
Becton Dickinson recalls SafeStep Huber Needle Sets with potential tubing cracks that could leak chemotherapy or blood. Affected units have specific catalog numbers and lot numbers. Stop using immediately to prevent exposure risks.
Becton Dickinson recalls SafeStep Huber Needle Set myPICK Port Access Kit with catalog numbers CPA00020A, CPA00042A, and CPA00049 due to potential tubing cracks causing chemical exposure risks.
Becton Dickinson recalls SafeStep Huber Needle Sets with specific catalog numbers due to potential tubing cracks causing chemical exposure and infection risks. Affected units include certain lot numbers and model variants.
Becton Dickinson recalls PowerLoc MAX Power Injectable Infusion Sets with potential tubing cracks that could leak chemotherapy or blood, risking infection or blood loss. Affected units have specific catalog numbers and lot numbers.
Becton Dickinson recalls PowerLoc MAX Power-Injectable Infusion Sets with potential tubing cracks near Luer/Y sites that could cause leaks of chemotherapy or blood, leading to infection or blood loss.
Becton Dickinson recalls SafeStep Huber Needle Set Port Access Kits with potential tubing cracks near Luer/Y sites, which could cause leaks of blood or chemotherapy. Affected units have specific catalog numbers and lot numbers.
Becton Dickinson recalls SafeStep Huber Needle Sets with PA-0031G model numbers due to tubing cracks that could leak chemotherapy or blood, risking infection or blood loss.
Recalled Becton Dickinson PowerLoc MAX Power Injectable Infusion Sets with specific catalog numbers and lot numbers due to potential cracks near Luer sites that could cause leaks of chemotherapy or blood, risking infection or blood loss.
Becton Dickinson recalls SafeStep Huber Needle Sets with Catalog CPA00040 due to potential tubing cracks causing chemical exposure and infection risks. Affected units include specific lot numbers.
Becton Dickinson recalls PowerLoc MAX Power Injectable Infusion Port Access Kits with specific catalog numbers and lot numbers due to potential tubing cracks causing chemical exposure or infection risks.
