--- title: "B. Braun Medical, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search B. Braun Medical, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/b-braun-medical-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # B. Braun Medical, Inc. recall records **240** reported ongoing 258 records in this archive. Latest source date Sep 3, 2026. 4 published notices do not supply a closure status. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Sep 3, 2026 FDA company announcement ### [B. Braun: 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container](https://isitonrecall.com/recall/fdapress-413d42dc0b0e4ebd-b-braun-0-9-sodium-chloride-injection-usp-100-ml-in-a-150-ml-pab-r-container/) Presence of particulate matter identified as iron oxide Not supplied Published notice; closure not supplied Distribution: Not supplied [Official source for B. Braun: 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/b-braun-medical-inc-issues-voluntary-nationwide-recall-09-sodium-chloride-injection-usp-100-ml-150) Aug 19, 2026 FDA drug enforcement ### [0.9% Sodium Chloride Injection, USP, 100 mL Partial Fill in 150 mL PAB Container, Sterile, Rx only, B. Braun Medical Inc., Bethlehem, PA 18018 USA, NDC 0264-1800-32.](https://isitonrecall.com/recall/fda-drug-d-0869-2026-0-9-sodium-chloride-injection-usp-100-ml-partial-fill-in-150-ml-pab-container-sterile-rx-only-b-brau/) Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene Class I Reported ongoing Distribution: Nationwide within the United States [Official source for 0.9% Sodium Chloride Injection, USP, 100 mL Partial Fill in 150 mL PAB Container, Sterile, Rx onl...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0869-2026%22) Aug 12, 2026 FDA drug enforcement ### [Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-00](https://isitonrecall.com/recall/fda-drug-d-0832-2026-lactated-ringer-s-injection-usp-1000-ml-excel-container-rx-only-l7500-b-braun-medical-inc-bethlehem/) Presence of Particulate matter. Class I Reported ongoing Distribution: U.S. Nationwide [Official source for Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical, Inc.,...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0832-2026%22) Aug 4, 2026 FDA device enforcement ### [Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025](https://isitonrecall.com/recall/fda-device-z-3089-2026-brand-name-extension-set-product-name-discofix-four-way-stopcock-model-catalog-number-456025/) Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of CA, CO, FL, GA, HI, IL, IN, LA, MA, MD, NC, NJ, NY, PA, TN, TX, VA, WA the country of Canada. [Official source for Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3089-2026%22) May 6, 2026 FDA device enforcement ### [Spinal Needle procedure kits: Material Description (Material Number) 24GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333867); 25GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333862); GOVP24...](https://isitonrecall.com/recall/fda-device-z-2276-2026-spinal-needle-procedure-kits-material-description-material-number-24ga-pencan-spinal-bup-tray-w-dura/) These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspe... Class I Reported ongoing Distribution: US Nationwide distribution. [Official source for Spinal Needle procedure kits: Material Description (Material Number) 24GA. PENCAN SPINAL BUP. TRA...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2276-2026%22) May 6, 2026 FDA device enforcement ### [Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spinocan 26 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333201); Sp...](https://isitonrecall.com/recall/fda-device-z-2277-2026-spinocan-spinal-needle-procedure-kits-material-description-material-number-spinocan-26-ga-x-3-1-2-in/) These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspe... Class I Reported ongoing Distribution: US Nationwide distribution. [Official source for Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spinocan 26 Ga. x ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2277-2026%22) May 6, 2026 FDA device enforcement ### [Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description (Material Number): SSK H M C 20061890 (560074), SSK S C H (560214), SSK BJC H S (ORIGINA...](https://isitonrecall.com/recall/fda-device-z-2278-2026-design-options-spinal-tray-spinal-needle-anesthesia-procedure-kits-material-description-material-num/) These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspe... Class I Reported ongoing Distribution: US Nationwide distribution. [Official source for Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description (Materia...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2278-2026%22) Apr 28, 2026 FDA drug enforcement ### [Lactated Ringer's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-07.](https://isitonrecall.com/recall/fda-drug-d-0540-2026-lactated-ringer-s-injection-usp-1000-ml-container-rx-only-b-braun-medical-inc-bethlehem-pa-18018-352/) Presence of Particulate Matter. Class I Reported ongoing Distribution: U.S.A. Nationwide [Official source for Lactated Ringer's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, P...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0540-2026%22) Apr 28, 2026 FDA company announcement ### [B. Braun: Lactated Ringer’s Injection, E7500, 1L](https://isitonrecall.com/recall/fdapress-143ec7c87165a01d-b-braun-lactated-ringer-s-injection-e7500-1l/) Products were found to contain particulate matter in solution Not supplied Published notice; closure not supplied Distribution: The product can be identified by product code E7500 or NDC 0264-7750-07. Product was distributed Nationwide to distributors, hospital, and healthcare facilities. [Official source for B. Braun: Lactated Ringer’s Injection, E7500, 1L](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/b-braun-medical-inc-issues-voluntary-nationwide-recall-lactated-ringers-injection-1l-e7500-due) Apr 2, 2026 FDA drug enforcement ### [Sterile Water for Injection USP, 3000 mL bags, Rx only, Pharmacy Bulk Package, B. Braun Medical Inc., Bethlehem, PA 18018-3524, NDC: 0264-7385-60.](https://isitonrecall.com/recall/fda-drug-d-0495-2026-sterile-water-for-injection-usp-3000-ml-bags-rx-only-pharmacy-bulk-package-b-braun-medical-inc-bethl/) Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. Class II Reported ongoing Distribution: US Nationwide. [Official source for Sterile Water for Injection USP, 3000 mL bags, Rx only, Pharmacy Bulk Package, B. Braun Medical I...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0495-2026%22) Apr 2, 2026 FDA drug enforcement ### [DEXTROSE INJECTION USP, 70%, 2000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7387-50.](https://isitonrecall.com/recall/fda-drug-d-0496-2026-dextrose-injection-usp-70-2000-ml-bags-rx-only-sterile-b-braun-medical-inc-bethlehem-pa-18018-3524-u/) Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. Class II Reported ongoing Distribution: US Nationwide. [Official source for DEXTROSE INJECTION USP, 70%, 2000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0496-2026%22) Apr 2, 2026 FDA drug enforcement ### [0.9 % SODIUM CHLORIDE IRRIGATION, USP, 3000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7388-60.](https://isitonrecall.com/recall/fda-drug-d-0497-2026-0-9-sodium-chloride-irrigation-usp-3000-ml-bags-rx-only-sterile-b-braun-medical-inc-bethlehem-pa-180/) Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. Class II Reported ongoing Distribution: US Nationwide. [Official source for 0.9 % SODIUM CHLORIDE IRRIGATION, USP, 3000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bet...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0497-2026%22) Apr 2, 2026 FDA drug enforcement ### [LACTATED RINGER'S IRRIGATION, 3000 mL bags, Sterile, Ex only, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7389-60.](https://isitonrecall.com/recall/fda-drug-d-0498-2026-lactated-ringer-s-irrigation-3000-ml-bags-sterile-ex-only-b-braun-medical-inc-bethlehem-pa-18018-352/) Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. Class II Reported ongoing Distribution: US Nationwide. [Official source for LACTATED RINGER'S IRRIGATION, 3000 mL bags, Sterile, Ex only, B. Braun Medical Inc., Bethlehem, P...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0498-2026%22) Mar 19, 2026 FDA device enforcement ### [B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG DR. Model Number: SL-2010M2096A.](https://isitonrecall.com/recall/fda-device-z-1798-2026-b-braun-hemodialysis-bloodlines-streamline-bloodline-set-for-dialog-dr-model-number-sl-2010m2096a/) Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. Class I Reported ongoing Distribution: Worldwide distribution - US Nationwide and the country of Canada. [Official source for B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG DR. Model Number: SL-2010M2...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1798-2026%22) Mar 19, 2026 FDA device enforcement ### [B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG. Model Number: SL-2010M2096](https://isitonrecall.com/recall/fda-device-z-1799-2026-b-braun-hemodialysis-bloodlines-streamline-bloodline-set-for-dialog-model-number-sl-2010m2096/) Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. Class I Reported ongoing Distribution: Worldwide distribution - US Nationwide and the country of Canada. [Official source for B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG. Model Number: SL-2010M2096](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1799-2026%22) Mar 19, 2026 FDA device enforcement ### [B. Braun Hemodialysis Bloodlines, STREAMLINE FRESENIUS FOR DAVITA. Model Number: SL-2000M2095DA.](https://isitonrecall.com/recall/fda-device-z-1800-2026-b-braun-hemodialysis-bloodlines-streamline-fresenius-for-davita-model-number-sl-2000m2095da/) Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. Class I Reported ongoing Distribution: Worldwide distribution - US Nationwide and the country of Canada. [Official source for B. Braun Hemodialysis Bloodlines, STREAMLINE FRESENIUS FOR DAVITA. Model Number: SL-2000M2095DA.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1800-2026%22) Mar 19, 2026 FDA device enforcement ### [B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model Number: SL-2000M2095L.](https://isitonrecall.com/recall/fda-device-z-1801-2026-b-barun-hemodialysis-bloodlines-streamline-bloodline-long-version-fmc-model-number-sl-2000m2095l/) Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. Class I Reported ongoing Distribution: Worldwide distribution - US Nationwide and the country of Canada. [Official source for B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model Number: SL-2000M2...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1801-2026%22) Mar 19, 2026 FDA device enforcement ### [B. Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 2.6MM PUMP SEGMENT. Model Number: B3-3632M3705.](https://isitonrecall.com/recall/fda-device-z-1802-2026-b-braun-hemodialysis-bloodlines-low-vol-no-chamber-2-6mm-pump-segment-model-number-b3-3632m3705/) Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. Class I Reported ongoing Distribution: Worldwide distribution - US Nationwide and the country of Canada. [Official source for B. Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 2.6MM PUMP SEGMENT. Model Number: B3-3632M3...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1802-2026%22) Mar 19, 2026 FDA device enforcement ### [B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT. Model Number: B3-4630M4705.](https://isitonrecall.com/recall/fda-device-z-1803-2026-b-braun-hemodialysis-bloodlines-low-vol-no-chamber-4-8mm-pump-segment-model-number-b3-4630m4705/) Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure. Class I Reported ongoing Distribution: Worldwide distribution - US Nationwide and the country of Canada. [Official source for B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT. Model Number: B3-4630M4705.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1803-2026%22) Feb 2, 2026 FDA device enforcement ### [Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF Model/Catalog Number: 7B3050 Software Version: N/A Product Description: A device designed for subcutaneou...](https://isitonrecall.com/recall/fda-device-z-1481-2026-brand-name-b-braun-product-name-bbraun-medical-21g-x4-4cm-winged-inf-model-catalog-number-7b3050-sof/) The potential for the needle tip to be dull/blunt, difficult to advance, and/or break. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the state of TX and the country of Costa Rica. [Official source for Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF Model/Catalog Number: 7B3...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1481-2026%22) ## Reasons in these listed records - Presence of particulate matter identified as iron oxide - Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene - Presence of Particulate matter. - Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label. These examples come from this result page and are not a ranking of every recall reason. ## Checking B. Braun Medical, Inc. ### Is there a recall on b. braun medical, inc. right now? This archive contains 258 records, including 240 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search B. Braun Medical, Inc.](https://isitonrecall.com/check/?q=B.%20Braun%20Medical%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)