B BRAUN MEDICAL INC recalls
Every recall we track for B BRAUN MEDICAL INC — 417 in all, from 2013–2026 — plus the complaints and injury reports the public filed about them. 28 are rated “stop using now”.
Recalls per year, by danger level
Recalls from B BRAUN MEDICAL INC more than doubled in 2025 (140, up from 53 in 2024). 6% rated “stop using now”.
All FDA recall records for B BRAUN MEDICAL INC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 1 | 9 | 1 | 11 |
| 2018 | 1 | 93 | 2 | 0 | 96 |
| 2019 | 0 | 2 | 13 | 3 | 18 |
| 2020 | 0 | 0 | 4 | 0 | 4 |
| 2021 | 1 | 17 | 1 | 0 | 19 |
| 2022 | 3 | 4 | 3 | 0 | 10 |
| 2023 | 5 | 10 | 8 | 0 | 23 |
| 2024 | 6 | 38 | 8 | 1 | 53 |
| 2025 | 6 | 118 | 15 | 1 | 140 |
| 2026 (to date) | 2 | 2 | 21 | 3 | 28 |
B BRAUN MEDICAL INC recalls before 2017
Recalls on record by year.
Most common reasons for B BRAUN MEDICAL INC recalls
What to do if you have a recalled B BRAUN MEDICAL INC product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All B BRAUN MEDICAL INC recalls
60 shown- Stop using nowDrug
B BRAUN MEDICAL INC recalls 0.9% Sodium Chloride Injection, USP, 100 mL Partial Fill in 150 mL PAB Container, Sterile, Rx only, B. Braun Medical
B. Braun Medical recalls 100mL sodium chloride injections with particulate matter (iron oxide, cellulose, polystyrene) in specific lots. Stop using if you have these lots.
B. Braun MedicalAug 19, 2026 - UnratedDrug
B BRAUN MEDICAL INC recalls Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical, Inc., Bethlehem, PA
B. Braun Medical recalls Lactated Ringer's Injection USP 1000mL (L7500) due to particulate matter. Affected units have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
B. Braun MedicalAug 12, 2026 - Lower riskMedical device
B Braun Medical Inc recalls Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025
B Braun recalls specific lots of Discofix Four Way Stopcock sets due to incorrect expiration date on carton labels. Affected units may have expired product.
B BraunAug 4, 2026 - Lower riskMedical device
B Braun Medical Inc recalls Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spinocan 26 Ga. x 3-1/2 in. (90 mm),
B Braun recalls Spinocan spinal needle kits with potential quality issues found during FDA inspection. Affected kits include specific sizes and batch numbers. Consumers should check their product details and contact the manufacturer.
B BraunMay 6, 2026 - Stop using nowDrug
B BRAUN MEDICAL INC recalls Lactated Ringer's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC
B. Braun Medical recalls 1000mL Lactated Ringer's Injection with particulate matter. Affected lots expire May 2027. Stop using immediately to avoid potential contamination.
B. Braun MedicalApr 28, 2026 - Lower riskDrug
B BRAUN MEDICAL INC recalls DEXTROSE INJECTION USP, 70%, 2000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC:
B Braun recalls 2000mL dextrose injection bags with potential contamination risk if foil is removed. Affected lots expire Nov 2026. Contact for return instructions.
B BraunApr 2, 2026 - Lower riskMedical device
B Braun Medical Inc recalls B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model Number: SL-2000M2095L.
B Braun recalls specific hemodialysis bloodlines due to potential air bubble accumulation in arterial lines under negative pressure. Affected models include StreamLine Bloodline Long Version (SL-2000M2095L) from June 2025 onward.
B BraunMar 19, 2026 - Lower riskMedical device
B Braun Medical Inc recalls Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 Software Version: N/A Product
B. Braun recalls 21GA Winged Inf Set model 7M2802 due to potential needle tip dullness or breakage during use. Affected units sold from 2020 to 2023 with specific lot numbers.
B. BraunFeb 2, 2026 - Lower riskMedical device
B Braun Medical Inc recalls Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK HARRIS METHODIST Model/Catalog Number: 555498 Software Version:
B. Braun Medical recalls CESK Harris Methodist model 555498 due to potential cracking of butyrate tubing, making the product unusable. Affected units may have specific lot codes.
B. Braun MedicalJan 29, 2026 - Use cautionMedical device
B Braun Medical Inc recalls Blood Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's
B Braun Medical recalls blood administration sets used with gravity IV pumps that may cause medication backflow into primary IV containers, risking contamination. Affected units have specific catalog numbers and are sold with certain pumps.
B Braun MedicalOct 29, 2025 - Use cautionMedical device
B BRAUN MEDICAL INC recalls Brand Name: Hemodialysis Bloodlines Product Name: STREAMLINE BLOODLINE SET FOR DIALOG Model/Catalog Number:
B. Braun recalls STREAMLINE BLOODLINE SET FOR DIALOG (model SL-2010M2096) due to potential micro-air bubbles in bloodlines causing alarm errors. Affected units include specific lot numbers listed in the recall.
B. BraunSep 30, 2025 - Use cautionMedical device
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged
B Braun recalls Perifix FX epidural anesthesia trays with potential incorrect catheter connector lid position. Affected units include specific lot numbers and expiration dates. Contact for remedy details.
B BraunSep 18, 2025 - Stop using nowDrug
B BRAUN MEDICAL INC recalls 0.9% SODIUM CHLORIDE IRRIGATION USP. ISOTONIC SOLUTION FOR IRRIGATION, 3000mL, Rx only, B. Braun Medical Inc.,
B Braun Medical recalls 3000mL 0.9% sodium chloride irrigation solution due to potential contamination from port leakage. Affected lots expire Feb 2027. Stop using immediately to prevent infection risks.
B Braun MedicalAug 26, 2025 - Use cautionDrug
B BRAUN MEDICAL INC recalls 0.9% Sodium Chloride Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA,
B. Braun Medical recalls 1000mL 0.9% Sodium Chloride Injection due to particulate matter risk. This IV fluid, sold Rx only, may cause serious injury if particles enter bloodstream.
B. Braun MedicalAug 18, 2025 - Lower riskDrug
B BRAUN MEDICAL INC recalls 0.9% Sodium Chloride Injection USP, L 8000, 1000mL Excel Container, Rx Only, Sterile, nonpyrogenic, single dose
B Braun Medical recalls 1000mL sterile 0.9% Sodium Chloride Injection due to potential contamination from fluid leakage at weld sites. Affected lots: J5C919 (expiring 08/31/2027).
B Braun MedicalAug 4, 2025 - Lower riskMedical device
B BRAUN MEDICAL INC recalls Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215. for use with IV tubing.
B Braun recalls Microbore Extension Sets with 0.2 Micron Filter (V6215) due to incorrect label claiming air-eliminating filter when it does not have an air vent.
B BraunJul 9, 2025 - Stop using nowDrug
B BRAUN MEDICAL INC recalls 0.9% Sodium Chloride Injection USP, 500 mL, packaged in 500 mL excel containers and further packaged 24 per case, Rx
B Braun recalls 500mL 0.9% Sodium Chloride Injection with pinholes in packaging that may cause leaks. Affected lots expire 2/28/2027. Stop using immediately to avoid contamination risks.
B BraunJun 16, 2025 - Lower riskDrug
B. Braun Medical Inc recalls 0.9% Sodium chloride Irrigation USP, Isotonic Solution for Irrigation, 500 mL Plastic Irrigation Container (PIC), B.
B. Braun Medical recalls 500mL isotonic saline containers with particulate matter risk. Affected lots: J4K936 (exp 7/31/2027). Contact for return instructions.
B. Braun MedicalMar 31, 2025 - Use cautionMedical device
B Braun Medical Inc recalls Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in., PUR, Winged. Passive safety IV catheter.
B Braun recalls Introcan Safety 3 IV catheters due to increased risk of valve housing detachment causing leakage. Affected models include 22 gauge, 1 inch, PUR, Winged catheters with specific serial numbers.
B BraunFeb 17, 2025 - Stop using nowMedical device
B. Braun Medical, Inc. recalls Design Options COMBINED SPINAL/EPIDURAL TRAY- Intended for administration of analgesic/anesthetic agent to intrathecal
B. Braun recalls combined spinal/epidural trays with incorrect catheter connector that can't securely administer medication. Affected units have model 530159 and UDI-DI 04046:696469286. Stop using immediately to prevent medication delivery failure.
B. BraunDec 4, 2024 - Use cautionMedical device
B Braun Medical Inc recalls SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to transfer blood between a patient and a haemodialyser during
B Braun recalls SL Bloodline tubing for FMC 2008 series to prevent occlusion during hemodialysis. Incomplete connector insertion may cause flow restrictions, requiring switch to retrograde flow.
B BraunAug 15, 2024 - Lower riskMedical device
B. Braun Medical, Inc. recalls AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold, Four-way Stopcock, Model/Catalog
B. Braun recalls anesthesia extension sets (model 472: 472036) due to potential leakage from the spin lock connector. Affected units were sold with specific lot numbers. Consumers should contact the company for details.
B. BraunAug 8, 2024 - Use cautionMedical device
B Braun Medical Inc recalls Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U
B Braun recalls certain Infusomat Space Infusion Systems for potential false occlusion alarms from electrostatic buildup during use. Affected pumps may need repair or replacement to prevent incorrect alerts.
B BraunAug 7, 2024 - UnratedDrug
B. Braun Medical Inc recalls 0.9% Sodium Chloride Injection USP, E8000, 1000mL container, Rx only, B. Braun Medical Inc., Irvine, CA, NDC
B. Braun Medical recalls 1000mL 0.9% Sodium Chloride Injection (Rx only) with lot numbers J2L763/J2L764, expiring March 2025, due to possible particulate matter. Consumers should contact the company for details.
B. Braun MedicalJul 24, 2024 - Use cautionMedical device
B. Braun Medical, Inc. recalls OUTLOOK PUMP SET 3 CARESITE LADS 133 IN.-Used with an electrically-powered infusion pump for intravenous (IV)
B. Braun recalls Outlook Pump Set 3 CareSite LADS 133 for potential medication backflow into IV containers, risking patient injury. Affected units distributed after August 22, 2:00 PM, 2023.
B. BraunJun 17, 2024 - Use cautionMedical device
B Braun Medical Inc recalls Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump, Wireless Model/Catalog Number: 8713031U Software
B Braun recalls Perfusor Space wireless syringe pumps with model 8713031U software due to incompatibility with Cardinal Health Monoject syringes, risking overdose or underdose in medical use.
B BraunJun 14, 2024 - Lower riskMedical device
B Braun Medical Inc recalls Stimuplex A, 30 DEG, 24GX1", 0.55x25mm, Catalogue Number: 4894251.
B Braun recalls Stimuplex A needles with DEHP traces in glue. These medical needles may cause health issues if used. Affected units have specific catalog numbers and batch dates.
B BraunMay 17, 2024 - Lower riskDrug
B. Braun Medical Inc recalls Lactated Ringer's Injection USP, 1000mL, EXCEL CONTAINER, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018, NDC
B. Braun Medical recalls 1000mL Lactated Ringer's Injection USP due to potential leakage causing contamination. Affected lots may pose sterility risks.
B. Braun MedicalMar 22, 2024 - Use cautionDrug
B. Braun Medical Inc recalls Potassium Chloride for Injection Concentrate USP, 500 mEq/250 mL (2 mEq/mL), 250 mL Bag, Rx only, B. Braun Medical
B. Braun Medical recalls Potassium Chloride for Injection Concentrate due to potential pinholes causing leaks. This affects specific lots and expiration dates. Consumers should contact the company for details.
B. Braun MedicalMar 6, 2024 - Lower riskMedical device
B. Braun Medical, Inc. recalls Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy, 5 mL Glass Luer Lock LOR Tray (Kit) A collection of devices
B. Braun recalls Epidural trays with Neuraxial connectors that prevent proper interface with other kit components. Affected units may cause improper administration of anesthesia. Contact for remedy details.
B. BraunJan 22, 2024 - Stop using nowMedical device
B. Braun Medical, Inc. recalls Infusomat Administration Sets as listed below: 362031 Infusomat Space Pump Set with Caresite Injection Site; 362032 15
B. Braun Medical recalls Infusomat Administration Sets with tubing size/length issues that may cause false air-in-line alarms, interrupting medication therapy and risking serious injury or death.
B. Braun MedicalNov 1, 2023 - Use cautionMedical device
B. Braun Medical, Inc. recalls TERUMO 60" TUBE SET W/HIGH CRACK CHK VLV, Article No. 7S3070. Singapore only. IV injection set.
B. Braun Medical recalls Singapore-only 60" IV tube sets with potential leakage causing infection or delayed therapy. Affected units include specific lot numbers.
B. BraunSep 26, 2023 - Stop using nowMedical device
B. Braun Medical, Inc. recalls 8713051U, Infusomat Large Volume Pump, Wireless; Volumetric Infusion Pump System
B. Braun recalls wireless Infusomat Large Volume Pumps with upstream occlusion alarms that may stop medication flow, risking hemodynamic instability or death. Affected units have specific serial numbers.
B. BraunSep 21, 2023 - Lower riskMedical device
B. Braun Medical, Inc. recalls B.Braun NORM-JECT Luer Lock Solo, 10 ml, Sterile-Intended to be used to deliver (inject) or withdraw an accurate
B. Braun recalls 10ml sterile NORM-JECT Luer Lock Solo syringes due to potential packaging damage that could compromise sterility. Affected units include specific lot numbers and distribution dates.
B. BraunAug 7, 2023 - Lower riskDrug
B. Braun Medical Inc. recalls 0.9% Sodium Chloride Injection USP, 1000 mL Excel Plus Container, Rx only, B. Braun Medical Inc. Bethlehem, PA 18018,
B. Braun Medical recalls 1000mL 0.9% Sodium Chloride Injection USP Excel Plus containers with missing or incomplete labeling. This affects prescription-only products sold with specific lot numbers.
B. Braun MedicalAug 2, 2023 - Lower riskMedical device
B. Braun Medical, Inc. recalls Perifix¿ / Epidural anesthesia set, medicated
B. Braun recalls medicated epidural anesthesia sets with possible incorrect lid stock labels. Affected units have specific UDI-DI and lot numbers. Consumers should check their product details to determine if recalled.
B. BraunJul 31, 2023 - Stop using nowDrug
B. Braun Medical Inc. recalls 0.9% Sodium Chloride Injection USP, 1000 mL Excel Plus Container, Rx only, B. Braun Medical Inc. Bethlehem, PA
B. Braun Medical recalls 1000mL 0.9% Sodium Chloride Injection (Excel Plus) due to potential leakage risks. Affected lots expire 3/31/2025. Contact for replacement.
B. Braun MedicalJul 5, 2023 - Lower riskMedical device
B. Braun Medical, Inc. recalls Design Options¿ / Epidural anesthesia kit (10 count carton)
B. Braun recalls some epidural anesthesia kits due to incorrect filter straw assembly. Affected kits include specific model numbers and lot numbers. Consumers should check their kits and contact the company for details.
B. BraunJun 5, 2023 - Lower riskDrug
B. Braun Medical Inc recalls Heparin Sodium, 25,000 USP units per 250mL, (100 USP units per mL) in 5% Dextrose injection, 250 ml Excel Container, B.
B. Braun Medical recalls heparin sodium injections with low anti-factor IIa potency. This may cause ineffective blood clotting. Affected products have specific lot numbers and expiration dates.
B. Braun MedicalMay 9, 2023 - Lower riskDrug
B. Braun Medical Inc recalls Heparin Sodium, 25,000USP units per 250 mL, (100 USP units per mL) in 5% Dextrose Injection, 250 mL Excel Container,
B. Braun Medical recalls heparin sodium injection with low anti-Factor IIa potency. This may cause ineffective blood clotting. Affected lots: J2C017, expires 9/30/2023.
B. Braun MedicalMar 1, 2023 - Use cautionDrug
B. Braun Medical Inc. recalls 0.9% Sodium Chloride Injection, USP, 500 mL Excel Plus Container, Rx Only, B. Braun Medical Inc. Bethlehem, PA 18018,
B. Braun Medical is recalling certain batches of 0.9% Sodium Chloride Injection for possible leakage due to incomplete seals. Affected lots have specific expiration dates and may exhibit microscopic channel leaks near the port assembly.
B. Braun MedicalFeb 10, 2023 - Lower riskDrug
B. Braun Medical, Inc. recalls 0.9% Sodium Chloride Injection USP 1000 mL Single-dose container Rx only NDC 0264-5802-00 B. Braun Medical Inc.
B. Braun Medical recalls 1000mL single-dose 0.9% Sodium Chloride Injection (NDC 0264-5802-00) due to potential leakage. This could compromise sterility. Contact for details.
B. Braun MedicalNov 25, 2022 - Stop using nowMedical device
B. Braun Medical, Inc. recalls CARESITE SMALLBORE EXT SET T-PORT 5 IN., Product Code 470114, 100 units per carton. The A6 Access Device is a valve
B. Braun Medical recalls 100 units per carton of CARESITE Smallbore Extension Set T-Port 5 in. due to high risk of leakage or detachment at bonded joints, potentially causing infections or life-threatening complications.
B. Braun MedicalSep 15, 2022 - Lower riskMedical device
B Braun Medical Inc recalls Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle device to provide venous or
B Braun recalls Introcan Safety FEP 14G catheters due to potential leakage at the hub. Affected units have specific product codes and expiration dates. Contact for return or repair.
B BraunSep 1, 2022 - Lower riskDrug
B. Braun Medical, Inc. recalls 0.9% Sodium Chloride Injection USP, 250 mL Excel Container, Rx only, B. Braun Medical Inc., Bethlehem, PA, NDC
B. Braun Medical recalls 250mL 0.9% Sodium Chloride Injection (Rx only) due to leaking bags that may cause contamination. Affected lots expire May 2023 or June 2023.
B. Braun MedicalFeb 25, 2022 - Use cautionMedical device
B Braun Medical Inc recalls PERFUSOR SPACE - US VERSION. Intended Use: syringe infusion pump that can be used to configure customized, tailor-made
B Braun recalls US version PERFUSOR SPACE infusion pumps with serial numbers 633299-633318 due to potential infusion errors. Affected units may cause delays, overinfusion, or underinfusion of medication.
B BraunFeb 7, 2022 - Use cautionMedical device
B. Braun Medical, Inc. recalls Dispensing Pins for Air Inlet Filter, Product Catalog No. 412005, DP2500 Dispensing Pin W/Valve. A valve for aspiration
B. Braun recalls DP2500 Dispensing Pins with potential leakage risk that could cause medication dose errors or bloodstream infections. Affected units have specific lot numbers and expiration dates.
B. BraunJan 31, 2022 - Use cautionMedical device
B Braun Medical Inc recalls Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems. Conductivity Sensor (END) - VERSION 2,
B Braun Medical recalls Conductivity Sensors (VERSION 2) for Dialog and Dialog+ hemodialysis systems due to potential cracks causing leaks that may lead to improper ultrafiltration. Affected units include specific model numbers and lots.
B Braun MedicalJan 28, 2022 - Use cautionMedical device
B. Braun Medical, Inc. recalls PUMP SET, 15 DR, 3 CARESITE, 127 in.single-use for use with the Outlook Safety Infusion System and/or Horizon NXT Pump
B. Braun recalls 15-dr 3-CareSite pump sets for potential medication leakage and bloodstream infections. Affected units sold with Outlook Safety Infusion System or Horizon NXT Pump.
B. BraunAug 10, 2021 - Use cautionMedical device
B. Braun Medical, Inc. recalls Infusomat Space Volumetric Pump Administration Set, Product Code 490100
B. Braun recalls Infusomat Space Volumetric Pump Administration Set (Product Code 490100) due to risk of unintended fluid flow if the anti-free flow clip is inverted. Affected units sold with Lot Number 0061761278.
B. BraunJun 25, 2021 - Lower riskMedical device
B. Braun Medical, Inc. recalls Filtered Triple-Leg Extension Set - Intravascular administration set. Product Catalog number: 477034 - Product Usage:
B. Braun recalls Filtered Triple-Leg Extension Set (catalog 477034) due to potential occlusion or inability to prime. Affected lots: 00SL713784, 0061741483, 0061755034, 0061755296.
B. BraunMar 15, 2021 - Lower riskMedical device
B Braun Medical, Inc. recalls APEX Compounding System Control Panel Module, REF: 601237, Product Code AX1000 - Product Usage: intended for
B Braun recalls APEX Compounding System Control Panel Module (AX1000) with software version 1.0.5.57 or earlier. The system may not detect air bubbles exceeding 3% of the ordered volume, risking inaccurate drug compounding.
B BraunNov 23, 2020 - Lower riskDrug
B. Braun Medical Inc recalls Ceftazidime for Injection USP and Dextrose for Injection USP, 2 g, 50 mL Duplex Container, RX only, B Braun Medical
B. Braun Medical recalls Ceftazidime for Injection USP and Dextrose for Injection USP, 2g/50mL, due to stability problems that could affect safety.
B. Braun MedicalApr 18, 2020 - Lower riskMedical device
B. Braun Medical, Inc. recalls Y-Type Blood Set, Catalog Number 490425
B. Braun recalls Y-Type Blood Set (Catalog 490425) due to potential leakage at blood filters and tubing joints. Affected units have specific lot numbers and expiration dates.
B. BraunNov 20, 2019 - Lower riskMedical device
B. Braun Medical, Inc. recalls CE17TKFCN EPID TRAY W/ 17GA TUOHY NRFIT Catalog # 339186
B. Braun recalls EPID trays with catalog #339186 due to potential filter membrane damage causing inadequate filter capacity. Affected units sold between 2018-2019.
B. BraunJul 10, 2019 - Lower riskDrug
B. Braun Medical Inc recalls Heparin Sodium 25,000 USP units per 250 mL (100 USP units per mL) in 5% Dextrose Injection, 250 mL EXCEL Container bag,
B. Braun Medical recalls heparin sodium 25,000 USP units per 250mL in 5% dextrose injection due to subpotent drug levels. This may cause ineffective blood thinning during medical procedures.
B. Braun MedicalJun 13, 2019 - Use cautionMedical device
B. Braun Medical, Inc. recalls B.Braun Infusomat Space Volumetric Infusion Pump Administration Set, Catalog Number 363032
B. Braun recalls specific infusion pump sets that may leak or disconnect at the Y-site joint, causing potential injury. Affected units have catalog number 363:032 and lot number 0061641410.
B. BraunMay 1, 2019 - Use cautionMedical device
B. Braun Medical, Inc. recalls CE17TKFSDTD EPID TRAY W/17GA FIXED WING, Material Number 332095 Connection device used by physicians to provide various
B. Braun recalls EPID trays with potential catheter connector leakage. Affected units have batch number 61580395. Stop using if leakage occurs.
B. BraunJul 20, 2018 - Lower riskMedical device
B. Braun Medical, Inc. recalls 26-Lead Transfer Set for use with APEX¿ Compounding System, Product Catalog Number 2112550
B. Braun recalls 26-Lead Transfer Sets for APEX Compounding System with potential for incorrect valve orientation causing unintended drug mixtures. Check product catalog numbers listed.
B. BraunJun 4, 2018 - Use cautionMedical device
B. Braun Medical, Inc. recalls Space Pump IV Set, 2 Caresites, ASV, 0.2 Micron Air Eliminating Filter, Product Code 363420 The Infusomat Space Pump IV
B. Braun recalls Space Pump IV sets with potential for incorrect filter that lacks air elimination. Affected units have lot number 0061583973. Consumers should check their IV sets for the filter and contact B. Braun for details.
B. BraunMay 9, 2018
B BRAUN MEDICAL INC recall questions
How many recalls has B BRAUN MEDICAL INC had?
417 recalls from B BRAUN MEDICAL INC are on record with U.S. safety agencies, from 2013–2026 (372 medical device, 45 drug).
What is the most recent B BRAUN MEDICAL INC recall?
B BRAUN MEDICAL INC recalls 0.9% Sodium Chloride Injection, USP, 100 mL Partial Fill in 150 mL PAB Container, Sterile, Rx only, B. Braun Medical, dated Aug 19, 2026. Every B BRAUN MEDICAL INC recall is listed on this page, newest first.
Why are B BRAUN MEDICAL INC products recalled?
The most common reasons on record: Potential for the lid of the catheter connector to be in the incorrect position. (13); The filter capacity is not achieved due to damage of the filter membrane. (9); Potential for leakage at the joint between the blood filters and tubing (7); Presence of Particulate Matter (3).
What should I do if I have a recalled B BRAUN MEDICAL INC product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new B BRAUN MEDICAL INC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.