Recalls in Nebraska (page 37)
3895 recalls.
- Rifton Equipment recall (Community Products, LLC)
Medical deviceClass IIReported January 28, 2026 · Potential for fraying on the body support strap. - Rifton Equipment recall (Community Products, LLC)
Medical deviceClass IIReported January 28, 2026 · Potential for fraying on the body support strap. - Rifton Equipment recall (Community Products, LLC)
Medical deviceClass IIReported January 28, 2026 · Potential for fraying on the body support strap. - TS-10/TS-10H Tube Sorter recall (Sysmex America, Inc.)
Medical deviceClass IIReported January 28, 2026 · Under specific conditions, the lift's electromagnetic holding force may disengage unexpectedly, allowing unintended downward movement of the lift. - Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius... recall (Tyber Medical)
Medical deviceClass IIReported January 28, 2026 · The supplier manufactured anatomical left plates with an incorrect thread orientation. - Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius... recall (Tyber Medical)
Medical deviceClass IIReported January 28, 2026 · The supplier manufactured anatomical left plates with an incorrect thread orientation. - Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number: MHR 110-b ... recall (LEASEIR TECHNOLOGIES SLU)
Medical deviceClass IIReported January 28, 2026 · The console label for affected devices is missing the "DANGER" symbol. - Mazor X robotic guidance system REF: TPL0059 recall (Mazor Robotics Ltd)
Medical deviceClass IIReported January 28, 2026 · Software errors that can result in incorrect surgical instrument positioning during spinal surgery. - SIGMA Spectrum Infusion Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported January 28, 2026 · Certain pumps have potentially been released from service with defective grease applied to the cam and motor gears. Due to its low viscosity, the defective... - ICU Medical Plum Solo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported January 28, 2026 · Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The programmed... - ICU Medical Plum Duo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported January 28, 2026 · Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The programmed... - ICU Medical Plum Duo Infusion Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported January 28, 2026 · Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The programmed... - GE Healthcare Omni Legend recall (GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING)
Medical deviceClass IIReported January 28, 2026 · There is a potential intermittent issue on certain Omni Legend systems that can result in a streaking artifact in the PET clinical scan images. This streaking... - Mikario Trading Convertible Baby Gyms Recalled Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standard for Infant Support Cushions; Sold on TikTok Shop
Consumer productReported January 22, 2026 · The recalled baby gyms violate the mandatory safety standard for infant support cushions because the floor mats can obstruct an infant's breathing, posing a... - Iristar Minoxidil Spray Bottles for Hair and Beard Growth Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Moralowen
Consumer productReported January 22, 2026 · The recalled spray bottles contain minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging is... - Aborder Products Recalls Cumbor Retractable Safety Gates Due to Risk of Serious Injury or Death to Children from Entrapment; Violates Mandatory Standard for Gates and Enclosures
Consumer productReported January 22, 2026 · The recalled gates violate the mandatory standard for expansion gates and expandable enclosures because a child's torso can fit through the opening between the... - Vndueey Magnetic Men Toy Sets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys
Consumer productReported January 22, 2026 · The recalled magnetic stick figure toy sets violate the mandatory standard for toys because the sets contain loose magnets, posing an ingestion hazard to... - Based Online Fidget Magnet Ball Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys
Consumer productReported January 22, 2026 · The magnet ball toys violate the mandatory standard for toys because they are loose high-powered magnets, posing an ingestion hazard to children. When... - Topkay Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Multipurpose Lighters; Sold on Amazon by Xiyude
Consumer productReported January 22, 2026 · The recalled lighters violate the mandatory standard for multipurpose lighters because they do not have the required child-resistant mechanisms, posing a risk... - Gagaku Children's Ice Cream Toy Playsets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion Hazard; Violate Mandatory Standard for Toys; Sold on Amazon by Brandworl.USA
Consumer productReported January 22, 2026 · The recalled toys violate the mandatory standard for toys because they contain high-powered magnets which can loosen and detach, posing an ingestion hazard to... - Yetonamr Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by Longyanguiheng
Consumer productReported January 22, 2026 · The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller than permitted. The silicone strings can reach the... - Johnson Health Tech Expands Recall to Include Matrix Retail and Vision Treadmills Due to Fire Hazard
Consumer productReported January 22, 2026 · The power cord can become loose from the treadmill's power socket, posing a fire hazard. - Academy Sports + Outdoors Recalls Magellan Odyssey Rocker Chairs Due to Injury and Fall Hazards
Consumer productReported January 22, 2026 · The recalled chairs' legs can break, posing injury and fall hazards to consumers. - Thrasio Recalls Angry Orange Enzyme Stain Removers Due to Risk of Exposure to Bacteria
Consumer productReported January 22, 2026 · The recalled products can contain bacteria, including Pseudomonas aeruginosa, an environmental organism found widely in soil and water. People with weakened... - Portex Spinal Tray recall (ICU Medical Inc.)
Medical deviceClass IIReported January 21, 2026 · Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may also lead to... - Pulsator Arterial Blood Sampling Kit recall (ICU Medical Inc.)
Medical deviceClass IIReported January 21, 2026 · Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may also lead to... - The product is used for the evaluation of the intrinsic coagulation pathway recall (Instrumentation Laboratory)
Medical deviceClass IIReported January 21, 2026 · Potential for microbial contamination. - Ivenix Infusion System recall (Fresenius Kabi USA, LLC)
Medical deviceClass IIReported January 21, 2026 · Emphasizing instructions for LVP duration programming located in the IFU. - FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle... recall (Abbott Diabetes Care, Inc.)
Medical deviceClass IReported January 21, 2026 · Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results - FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle... recall (Abbott Diabetes Care, Inc.)
Medical deviceClass IReported January 21, 2026 · Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results - FreeStyle Libre 3 Plus Sensor REF 78768-01 UDI-DI code: 00357599844011 The FreeStyle... recall (Abbott Diabetes Care, Inc.)
Medical deviceClass IReported January 21, 2026 · Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results - FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre... recall (Abbott Diabetes Care, Inc.)
Medical deviceClass IReported January 21, 2026 · Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results - HerbsForever- Hingwastika Churna recall (Herbs Forever)
FoodClass IReported January 21, 2026 · Potential undeclared allergen ingredient (Wheat) - HerbsForever- Gastro Care recall (Herbs Forever)
FoodClass IReported January 21, 2026 · Potential undeclared allergen ingredient (Wheat) - Jumbo RAW SHRIMP recall (AZ Gems, Inc.)
FoodClass IIReported January 21, 2026 · elevated levels of chloramphenicol in frozen shrimp - So Delicious Dairy Free Salted Caramel Cluster Cashewmilk recall (WhiteWave - Louisville Pilot Plant)
FoodClass IIReported January 21, 2026 · Foreign material - Lanreotide Injection recall (Cipla USA, Inc.)
DrugClass IIReported January 21, 2026 · Presence of Particulate Matter. - Toothpaste: a) COLGATE recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Deodorant: a) Axe recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Petroleum jelly: a) Vaseline Petroleum Jelly recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - LUCKY ICE recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Personal Care recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Carmex a) jar recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Personal Care recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Swan recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - TUMS a) Assorted recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Halls Cough Drops a) BAGS recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - TYLENOL a) 500 MG. recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - PEPCID COMPLETE - 25CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - PEPTO BISMOL 32CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - CHILDREN NYQUIL recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - NYQUIL COLD & FLU -32CT/2PK recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - LIQUID NYQUIL a) regular recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - MOTRIN 2'S DISP.- 50CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - EXCEDRIN MIGRAINE 2'S- 25 CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - EXCEDRIN 2'S DISP.- 30 CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - LIQUID DAYQUIL 12/8oz recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - DAYQUIL COLD & FLU recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Claritin recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Bayer 2Pk- 25 CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Benadryl recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Alka Seltzer recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Aleve 1's recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Advil a) Ibuprofen recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - AQ 120 GFEW recall (Encon Safety Products Co)
DrugClass IIReported January 21, 2026 · cGMP deviations. - Levothyroxine Sodium Tablets recall (Alvogen, Inc)
DrugClass IIReported January 21, 2026 · Product Mix-Up: A single bottle of this lot was reported by a pharmacy to contain 88 mcg tablets instead of 150 mcg tablets. - Clindamycin Phosphate USP recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported January 21, 2026 · Failed Impurities/Degradation: Out of Specification results for Total Impurities and for Assay. - Fluocinolone Acetonide Solution Topical Solution USP recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported January 21, 2026 · Failed Impurities/Degradation Specifications: Out of specification result was obtained for the known impurity D. - Abre Venous Self-Expanding Stent System recall (Medtronic Inc)
Medical deviceClass IIReported January 21, 2026 · Stents may be impacted by a Nitinol anomaly which causes a reduced stent diameter when deployed and corresponding reduced radial force. Issue may result in... - da Vinci SP recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported January 21, 2026 · Access Port System tray may develop cracks potentially resulting in a sterility breach. - Plum Duo Infusion System recall (ICU Medical, Inc.)
Medical deviceClass IIReported January 21, 2026 · ICU Medical received one lot of defective primary speakers from our supplier that may fail to produce an audible sound. If the primary speaker in your Plum Duo... - ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution. recall (Hologic, Inc)
Medical deviceClass IIReported January 21, 2026 · Fungal contamination of affected lot with Parengyodontium album. - Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes the... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Six (6) identified software issues which may result in the following: system keeps restarting, AMC triple drive, C-Partition of Suite PC running out of free... - Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY PROSTATE recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Medline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Medline medical procedure convenience kits labeled as: 1) ROBOTIC recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Medline medical procedure convenience kits labeled as: 1) WCH BARI-GASTRECTOMY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and... - Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is... recall (Diagnostica Stago, Inc.)
Medical deviceClass IIReported January 21, 2026 · Potential for defect for Asserachrom HPIA lot 271288, which can affect every well in the impacted strip and produce negative results. - Philips Azurion Systems R3.0. Includes the following label descriptions and... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Nine (9) identified software issues which may result in the following: loss of X-ray after Pedal Tap, loss of X-ray after Phase Fault, missing live X-ray on... - MOSAIQ Oncology Information System with Particle Therapy License recall (Elekta, Inc.)
Medical deviceClass IIReported January 21, 2026 · Using oncology information system that manages workflow may result in overtreatment if:Plan delivered with Particle Therapy IHE-RO TDW-II interface,With one... - Allura Xper FD20/20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 Biplane recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 Biplane recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Allura Xper FD10F recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - Product Name: Allura Xper FD10C recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections... - BD Ready-to-Use Hydrophilic Catheter 14 Fr recall (HANGZHOU BEVER MEDICAL DEVICES CO., LTD.)
Medical deviceClass IIReported January 21, 2026 · Labeling error, Incorrect expiration date - Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets recall (Medline Industries, LP)
Medical deviceClass IIReported January 21, 2026 · Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check...