Every recall we track for B BRAUN MEDICAL INC — 415 in all — plus the complaints and injury reports the public filed about them.
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 Medical recalls certain spinal needle anesthesia procedure kits due to potential quality issues identified during FDA inspection. Affected kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP.
Braun Medical recalls spinal needle procedure kits containing Bupivacaine Hydrochloride due to potential quality issues identified during FDA facility inspections. Affected kits have specific material numbers and batch numbers.
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. 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 Medical recalls 3000mL sterile water bags due to potential contamination risk if foil is removed. Affected lots expire May 2028 and April 2028. Consumers should check lot numbers and contact the company for details.
B Braun Medical recalls sterile saline bags with potential contamination risk if foil is removed. Affected lots expire April 2028. Stop using if you have these specific lot numbers.
B Braun recalls 3000mL sterile lactated ringer's irrigation bags with potential contamination risk if foil is removed. Affected lots expire April 2028 or May 2028. Stop using if you have these specific lots.
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 Braun recalls STREAMLINE BLOODLINE SET FOR DIALOG (model SL-2010M2096) due to potential air bubble accumulation in arterial lines during hemodialysis. Affected units were manufactured from May 25, 2025.
B Braun recalls low-volume hemodialysis bloodlines with potential air bubble accumulation in arterial lines due to blood gas adherence. Affected model B3-3632M3705 (all lots since Aug 2025) may cause complications during dialysis.
B Braun recalls specific hemodialysis bloodlines (model B3-4630M4705) due to potential air bubble accumulation in arterial lines under negative pressure. Affected units manufactured since August 5, 2025.
B Braun recalls specific hemodialysis bloodlines (SL-2000M2095DA) due to potential air bubble accumulation in arterial lines during dialysis, which could cause complications.
B Braun recalls STREAMLINE BLOODLINE SET for Dialog DR. Model SL-2010M2096A due to potential air bubble accumulation in arterial lines during hemodialysis. Affected units manufactured since June 9, 2025.
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. Braun recalls 21G X4.4CM Winged Infusion Needles (model 7B3050) due to potential needle tip dulling, which may cause difficulty advancing or breaking during use. Affected units include specific lots with expiration dates through April 2032.
B. Braun recalls 21GA Winged Infusion needles (model 7A3842) due to potential dullness leading to breakage during use. Affected units include specific lots with expiration dates through June 2032.
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. Braun Medical recalls SESK UPMC Double Catheter Tray model 530134 due to potential cracking of butyrate tubing, making the product unusable. Affected units may need replacement.
B. Braun Medical recalls CESK Riverside Health System software model 552126 due to potential cracking of butyrate tubing that makes the product unusable. Affected units sold with specific lot codes.
B. Braun recalls spinal epidural pump model 530184 due to potential butyrate tubing cracking that makes it unusable. Affected units sold to hospitals, including Lyndon B Johnson Hospital.
B. Braun Medical recalls BPSK Blockjocks Tray model 570246 due to potential cracking of butyrate tubing that makes the product unusable. Affected units may need replacement.
B. Braun recalls NES1725KFXL spinal epidural catheters due to potential butyrate tubing cracks that make the product unusable. Affected units were sold with model 530201.
B. Braun recalls CESK SHANDS Jackson 20055717 model 555884 due to potential butyrate tubing cracking, making it unusable. Affected units sold in 2023.
B. Braun Medical recalls CESK Northside Anesthesia Trays with model 555076 due to potential butyrate tubing cracking, making the product unusable. All units have been returned as of January 2026.
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 recalls Outlook IV sets used with Infusomat pumps due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and expiration dates.
B Braun Medical recalls IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and pump models.
B Braun Medical recalls specific IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units include model 490:04046964186042.
B Braun recalls specific IV extension sets used with Infusomat pumps due to potential medication backflow and inability to prime. Affected units have catalog number 474912.
B Braun Medical recalls anesthesia IV sets that may cause medication backflow between IV containers, risking incorrect dosing. Affected sets include specific models sold with Infusomat pumps.
B Braun recalls gravity and pump IV sets used with Infusomat Space pumps due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and are sold with certain pump models.
B Braun recalls specific IV administration sets used with pumps due to potential medication backflow and inability to prime. Affected units include those with catalog number 480:231.
B Braun recalls specific IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units have catalog numbers 477002 or 477017.
B Braun Medical recalls specific IV administration sets used with gravity and pump systems due to potential backflow of medication and inability to prime. Affected units include catalog number 490208.
B Braun Medical recalls IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and expiration dates.
B Braun recalls specific IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units have catalog number 457:504.
B Braun Medical recalls SafeDAY IV sets used with Infusomat pumps due to potential medication backflow and inability to prime. Affected units include specific catalog numbers and expiration dates.
B Braun Medical recalls blood administration sets used with certain IV pumps due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and pump models.
B Braun Medical recalls IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and expiration dates.
B Braun recalls specific IV extension sets used with Infusomat pumps due to potential medication backflow and inability to prime. Affected units include catalog numbers 490448, 490465, 490486, and 490577.
B Braun recalls specific IV burette sets that may cause medication backflow between IV containers, risking contamination. Affected units include those with catalog number 490159 sold with Infusomat pumps.
B Braun recalls CARESAFE IV administration sets used with Infusomat pumps due to potential medication backflow and inability to prime, which could cause serious injury during IV therapy.
B Braun recalls specific IV administration sets that may cause medication backflow and inability to prime, potentially leading to incorrect dosing. Affected sets include models with catalog numbers 354209, 490392, and 490428.
B Braun recalls ULTRASITE IV sets used with Infusomat pumps due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and expiration dates.
B Braun Medical recalls specific IV administration sets used with gravity and pump systems due to potential backflow of medication and inability to prime. Affected units have catalog numbers 490312 and 490432.
B Braun recalls gravity IV sets with CARESITE injection sites due to potential medication backflow into primary IV containers and inability to prime. Affected units include specific catalog numbers and pump models.
B Braun recalls IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units include specific models sold with Infusomat Space, Outlook, and Vista pumps.
B Braun Medical recalls Outlook IV sets used with Infusomat pumps due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and expiration dates.
B Braun recalls IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and expiration dates.
B Braun Medical recalls anesthesia IV sets used with certain pumps due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and are sold with Infusomat, Outlook, and Vista pumps.
B Braun recalls certain IV extension sets used with Infusomat pumps due to potential medication backflow and inability to prime. Affected sets have specific catalog numbers and are sold with certain pump models.
B Braun Medical recalls IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units include specific catalog numbers for gravity IV sets.
B Braun recalls IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and pump models.
B Braun recalls anesthesia IV sets that may cause medication backflow between IV containers, risking contamination. Affected sets include specific models sold with Infusomat pumps. Stop using immediately to prevent potential contamination.
B Braun recalls specific IV extension sets used with Infusomat pumps due to potential medication backflow and inability to prime. Affected units have catalog number 490:629. Stop using immediately to prevent medication contamination.
B Braun recalls specific IV administration sets used with gravity and pump systems due to potential backflow of medication and inability to prime. Affected units include those with catalog number 490:317.
B Braun Medical recalls IV administration sets used with gravity and pump systems due to potential medication backflow and inability to prime. Affected units have specific catalog numbers and expiration dates.
B Braun Medical recalls IV administration sets used with gravity and pump systems due to potential backflow of medication and inability to prime. Affected units have specific catalog numbers.
B Braun recalls extension sets for IV pumps that may cause medication backflow between IV containers, risking contamination. Affected units have specific catalog numbers and pump models.
