Recalls in Nebraska (page 17)
3895 recalls.
- Lacosamide Tablets recall (Annora Pharma Private Limited)
DrugClass IIReported July 1, 2026 · Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg. - BD ChloraPrep FREPP Clear recall (CareFusion 213, LLC)
DrugClass IReported July 1, 2026 · Non-Sterility: Due to presence of Aspergillus penicillioides. And Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the... - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IReported July 1, 2026 · Non-Sterility: Due to presence of Aspergillus penicillioides. - BD ChloraPrep FREPP Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 1, 2026 · Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area. - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 1, 2026 · Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area. - hydrOXYzine Hydrochloride Oral Solution recall (ANI Pharmaceuticals, Inc.)
DrugClass IIIReported July 1, 2026 · Presence of foreign substance - DULOXETINE D/R recall (Direct Rx)
DrugClass IIReported July 1, 2026 · CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit - Sensipar recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Corlanor recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · Presence of Foreign Substance. - Sensipar recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Sensipar recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Corlanor recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · Presence of Foreign Substance. - Fenofibrate Capsules recall (Ajanta Pharma USA Inc)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Carton Label: MAJOR recall (The Harvard Drug Group LLC)
DrugClass IIReported July 1, 2026 · Subpotent Drug - Abiomed Impella CP Set with SmartAssist recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed Impella CP Set with SmartAssist recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product... recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP. Impella Set Product... recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 1, 2026 · There is the potential for leakage along the drug pathway from the pump through the end of the catheter. - Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following... recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure... - Octopus 4 Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Octopus Evolution AS Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Octopus Evolution Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser. recall (IPG Medical Corporation)
Medical deviceClass IIReported July 1, 2026 · Software anomaly that causes a false display of error code 5018. - GE Healthcare AW Server 3.2 ext.6.5 recall (GE Medical Systems SCS)
Medical deviceClass IIReported July 1, 2026 · GE HealthCare has become aware of a context synchronization issue in AW Server 3.2 ext. 6.5. When a user selects a patient or exam in the AW Server Web Client... - Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe... recall (Acumed LLC)
Medical deviceClass IIReported July 1, 2026 · Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use. - Off-Axis Alliance Glenoid recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Alliance Glenoid recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Comprehensive Shoulder System recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Comprehensive Shoulder System recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Comprehensive Shoulder System Small recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Multi-Snare Set: 5 mm x 125 cm recall (PFM MEDICAL INC.)
Medical deviceClass IIReported July 1, 2026 · A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility... - VOCSN+Pro package recall (Ventec Life Systems, Inc.)
Medical deviceClass IIReported July 1, 2026 · Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which... - TMJ Bilateral Implants recall (TMJ Solutions Inc)
Medical deviceClass IIReported July 1, 2026 · Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided... - Philips Avalon Fetal Monitor recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or... - Philips Avalon Fetal Monitor recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or... - Da Vinci ASSY recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported July 1, 2026 · Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would... - Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - Medline Convenience Kits: 1) DRAWER 6 CENTRAL LINE INSERTIO recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - Medline Convenience Kits: 1) OPEN HEART CDS recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - Medline Convenience Kits: 1) DYNJ905503F recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - Combination Smoke and Carbon Monoxide (CO) Detectors Recalled Due to Risk of Serious Injury or Death from Failure to Alert Consumers to Fire; Sold Exclusively on Amazon.com by Treatlife Technology
Consumer productReported June 30, 2026 · The recalled detectors can fail to alert consumers of a fire, posing a risk of serious injury or death from smoke inhalation or burns. - Daikin Comfort Technologies Manufacturing Recalls Amana Air Conditioners and Heat Pumps Due to Risk of Serious Injury from Fire and Burns
Consumer productReported June 30, 2026 · The heating element can remain energized during a ground fault, despite being turned off, posing a risk of fire or burn injury to consumers. - Honlyne LED Party Favors Recalled Due to Risk of Serious Injury Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries; Sold by Huizhou Rongheng Network Technology
Consumer productReported June 30, 2026 · The LED party favors violate the mandatory safety standard for consumer products because the battery compartment within the light-up products contains button... - Montessori Busy Board Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Small Fish
Consumer productReported June 30, 2026 · The busy boards violate the mandatory safety standard for toys because magnets can detach, posing a deadly ingestion hazard. When high-powered magnets are... - Raychy Children's Light Sneakers Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Coin Batteries; Imported by Carina and Rambo
Consumer productReported June 30, 2026 · The recalled sneakers violate the mandatory standard for consumer products with button cell and coin batteries because the lithium coin batteries can be... - Shield Line Recalls MedPride Baby Oil Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging
Consumer productReported June 30, 2026 · The baby oil contains low-viscosity hydrocarbons, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The baby... - Southern Telecom Expands Recall of Lomi Waxing Kits Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Additional Model and Reported Incidents
Consumer productReported June 30, 2026 · The roll-on warmers' power cord can overheat and short circuit, posing a risk of serious injury or death from fire, burn and electrical shock hazards. - Super Off-Road Solar Power Banks Recalled Due to Overheating; Imported by Spector & Co.
Consumer productReported June 30, 2026 · The solar power bank's lithium-ion battery can swell and overheat, posing a burn hazard to consumers. - Yamazuki Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury or Death from Crash; Violate Mandatory Standard for ATVs
Consumer productReported June 30, 2026 · The recalled youth ATVs violate the mandatory safety standard for ATVs because they are missing brake lights, reducing visibility of the youth ATV to other... - Kith Retail Recalls Children's Loungewear Sets Due to Risk of Serious Injury from Burn Hazard; Violate Mandatory Standards for Children's Sleepwear
Consumer productReported June 30, 2026 · The recalled children's loungewear sets violate the mandatory flammability standards for children's sleepwear, posing a risk of serious burn injuries. - Great Value Hawaiian Roll 4pk recall (United States Bakery)
FoodClass IIReported June 24, 2026 · Firm observed oily and sticky substance on direct food contact surface packaging of finished product. - Nutrisystem recall (Nutrisystem Inc)
FoodClass IIReported June 24, 2026 · Undeclared Allergen (Soy) - Brand Name: HeartMate Product Name: HM 11V Li-ion Backup Battery recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - Brand Name: HeartMate Product Name: HeartMate 3" System Controller Model/Catalog... recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta"... recall (BD SWITZERLAND SARL)
Medical deviceClass IIReported June 24, 2026 · Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening... - Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product... recall (Staar Surgical AG)
Medical deviceClass IIReported June 24, 2026 · Due to a software coding issues for calculating the implant orientation diagram printout for the implantation for toric implantable collamer lenses. - Impella CP Set with SmartAssist. Product Codes: 1000080 recall (Abiomed, Inc.)
Medical deviceClass IReported June 24, 2026 · Exposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of mechanical... - Description/REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: CVC KIT: 16 GA X 8IN/AK-04210 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PICC ACCESS TRAY/ASK-04001-CG1 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: MIDLINE CATHETER KIT: 3 FR X 20 CM/CDC-02031-MK1A recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PSI KIT: 7 FR X 4 IN/ASK-09701-UP recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/ASK-04001-MC3 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-SPC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: SAC KIT: 18 GA X 12CM W BIO/SAC-01218-B recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: SPINAL ANESTHESIA KIT/ASA-24090-SB recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PARACENTESIS KIT/ASK-00376-JHH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/GU-04020 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/ASK-04001-JHH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PACING/PSI KIT: 5 FR 2L/ASK-07155-MGU recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: DRAINAGE KIT/AK-01600 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-12122-F recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM6 RA CATH KIT: 20 GA X... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality...