Recalls in Mississippi (page 20)
3949 recalls.
- DOXOrubin Hydrochloride Liposome injection recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IReported June 17, 2026 · Presence of Particulate matter: Particulate matter identified as glass. - Orca Single Use Air/Water and Suction Valves recall (Boston Scientific Corporation)
Medical deviceClass IIReported June 17, 2026 · Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence... - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - MOSAIQ Oncology Information System recall (Elekta, Inc.)
Medical deviceClass IIReported June 17, 2026 · Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs. - Boston Scientific Model SC-4318 recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported June 17, 2026 · Sterile anchors my lack sterility assurance. - Boston Scientific TCN Electrodes: REF: TCN-5 recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported June 17, 2026 · Reusable electrodes may not meet expected performance levels. - Boston Scientific CSK Electrodes: REF: CSK-TC10 recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported June 17, 2026 · Reusable electrodes may not meet expected performance levels. - Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit recall (Inter-Med Llc)
Medical deviceClass IIReported June 17, 2026 · Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different... - Hintermann Series Talar Implant recall (DT MedTech, LLC)
Medical deviceClass IIReported June 17, 2026 · Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant... - Siemens Dimension Tacrolimus Flex Reagent Cartridge recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported June 17, 2026 · A potential positive bias in quality control (QC) and patient sample results in three lots of the Dimension Tacrolimus (TAC) Flex reagent cartridge. - Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number:... recall (The Binding Site Group, Ltd.)
Medical deviceClass IIReported June 17, 2026 · It was reported that plates 2 and 3 were marked as passed , although it appeared that QC had not been performed on these plates, despite samples being... - Medartis APTUS recall (Medartis AG)
Medical deviceClass IIReported June 17, 2026 · The cannulation of the CCS screw is not centered. - NexxZr T Multi A3.5 W98-16mm recall (Sagemax Bioceramics, Inc.)
Medical deviceClass IIReported June 17, 2026 · Yttrium-stabilized zirconium oxide discs for fixed all-ceramic dental restorations may have reduced or missing dentin layer and when used clinically in the... - SD LTM 64 PLUS recall (Micromed S.p.A.)
Medical deviceClass IIReported June 17, 2026 · Natus has become aware of two complaints related to the SD LTM 64 PLUS where the EEG traces acquired from two or four different amplifiers used in a multiple... - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number:... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - CGuard¿ Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - CGuard Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - Brand Name: CGuard Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - CGuard Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - Brand Name: CGuard¿ Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - Brand Name: CGuard¿ Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - TDC VELOCE" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)
Medical deviceClass IIReported June 17, 2026 · An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. - TDC VELOCE" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)
Medical deviceClass IIReported June 17, 2026 · An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. - TDC VELOCE" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)
Medical deviceClass IIReported June 17, 2026 · An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. - Bicarby" Dialysate recall (Fresenius Medical Care Holdings, Inc.)
Medical deviceClass IIReported June 17, 2026 · Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the... - EXCOR Pediatric Ventricular Assist Device recall (BERLIN HEART GMBH)
Medical deviceClass IIReported June 17, 2026 · Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures. - Mahurkar Elite PASS Trays recall (Mozarc Medical US LLC)
Medical deviceClass IIReported June 17, 2026 · The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays. - Allia Moveo angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS 7 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS 5 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS 3 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Plum Duo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and... - Plum Duo Infusion Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and... - Plum Solo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and... - Coffeemakers Recalled Due to Risk of Serious Injury from Burn Hazard; Imported by Kidisle
Consumer productReported June 12, 2026 · The recalled coffeemakers can become clogged, causing hot liquid or steam to build up and be released unexpectedly during use, posing a risk of serious injury... - Yamaha Recalls UMAX Bistro and Bistro Deluxe Vehicles Due to Injury Hazard
Consumer productReported June 12, 2026 · The recalled Bistro and Bistro Deluxe vehicles have an inaccurate weight capacity certification label. This could result in the vehicle being overloaded, which... - Houoto 642-2150V Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Prosperity goes straight up
Consumer productReported June 12, 2026 · The drain covers do not bear the required product markings, in violation of the mandatory safety standard under the Virginia Graeme Baker Pool and Spa Safety... - Arctic Zone Titan Pro Coolers Recalled Due to Risk of Serious Injury or Death from Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
Consumer productReported June 12, 2026 · The recalled children's pajamas violate the mandatory flammability safety standard for children's sleepwear, posing a risk of serious burn injuries or death to... - Arctic Zone Titan Pro Coolers Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Imported by California Innovations and Sold at Costco
Consumer productReported June 12, 2026 · The recalled coolers' latch magnet can detach, posing risk of serious injury or death from a choking hazard. - 7-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon.com by Hasuit Direct
Consumer productReported June 12, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Nimood Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation Hazards; Violate Mandatory Standard for Adult Portable Bed Rails
Consumer productReported June 12, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails, because users can become entrapped within the bed rail or between the bed... - Kawasaki Motors USA Recalls Model Year 2026 Teryx4 H2 and Teryx5 H2 Recreational Off-Road Vehicles Due to Impact and Injury Hazards
Consumer productReported June 12, 2026 · The drive converter sheave can break in certain circumstances, resulting in metal fragments being discharged within the engine compartment and surrounding... - Hopelight Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by MOCCI SHOP
Consumer productReported June 12, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed... - Yamaha Recalls Model Year 2021-2022 Fleet Golf Cars Due to Risk of Serious Injury or Death from a Crash Hazard
Consumer productReported June 12, 2026 · The recalled golf cars' passenger-side brake cable could have been misrouted during assembly. If the cable was misrouted, abnormal wear can occur which can... - Timechee Changing Table Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by Timechee
Consumer productReported June 12, 2026 · The recalled dressers are unstable if not anchored to the wall, posing tip-over and entrapment hazards that can result in a risk of serious injuries or death... - School Specialty Recalls Tip Restraint Kits Included in Childcraft Furniture Due to Risk of Serious Injury or Death from Tip-Over Hazard
Consumer productReported June 12, 2026 · The recalled plastic tip restraint kits (also referred to as furniture straps) can break or degrade, posing tip-over and entrapment hazards. Should the... - Merkury Innovations Recalls Hot + Cool Heating and Cooling Fans Due to Risk of Serious Injury or Death from Fire Hazard
Consumer productReported June 12, 2026 · The fan can overheat, posing a risk of serious injury or death from a fire hazard. - LiKee Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by ChilanTech
Consumer productReported June 12, 2026 · The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach... - HSN Recalls Kitchen HQ Thermal Insulated Bowls Due to Fire Hazard
Consumer productReported June 12, 2026 · Metal springs in the detachable hinged lid of the insulated bowls can catch fire when used in the microwave, posing a fire hazard. - Joyin Recalls Sloosh Dive Sticks Due to Risk of Serious Injury from Impalement; Violate Federal Dive Sticks Ban
Consumer productReported June 12, 2026 · The recalled dive sticks violate the federal dive sticks ban because they exceeded the compress limit, posing an impalement hazard. In shallow water, children... - Cold Prep Cream Sauce recall (The Coffee Connexion Co., Inc)
FoodClass IReported June 10, 2026 · Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination - Alfredo Sauce recall (The Coffee Connexion Co., Inc)
FoodClass IReported June 10, 2026 · Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination - Aramark Cheese Sauce New & Improved recall (The Coffee Connexion Co., Inc)
FoodClass IReported June 10, 2026 · Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination - 1) Cheese Sauce Mix recall (The Coffee Connexion Co., Inc)
FoodClass IReported June 10, 2026 · Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination - Brand Name: Da Vinci 5 Product Name: ASSY recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported June 10, 2026 · Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions... - Digital Angiography System Trinias:UD150G-40 / D150GC-40 recall (Shimadzu Medical Systems)
Medical deviceClass IIReported June 10, 2026 · Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off. - Arvis Hip & Knee 2.0 Instrument Set recall (Kico Knee Innovation Company)
Medical deviceClass IIReported June 10, 2026 · The Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face. - Arvis Hip & Knee 3.0 Instrument Set recall (Kico Knee Innovation Company)
Medical deviceClass IIReported June 10, 2026 · The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face. - PhaseOne Antimicrobial Solution recall (Oculus Technologies of Mexico, S.A. de C.V.)
Medical deviceClass IIReported June 10, 2026 · The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material... - The Large Volume Pump recall (Fresenius Kabi USA, LLC)
Medical deviceClass IIReported June 10, 2026 · Potential for the Cassette Loading Lever to break. - Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050 recall (Covidien LLC)
Medical deviceClass IIReported June 10, 2026 · Temperature probe devices lack FDA clearance. - Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044 recall (Covidien LLC)
Medical deviceClass IIReported June 10, 2026 · Temperature probe devices lack FDA clearance. - Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042 recall (Covidien LLC)
Medical deviceClass IIReported June 10, 2026 · Temperature probe devices lack FDA clearance. - Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number:... recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported June 10, 2026 · Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow... - BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - Ivenix Infusion System recall (Fresenius Kabi USA, LLC)
Medical deviceClass IReported June 10, 2026 · Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may... - LVP software of the Ivenix Infusion System recall (Fresenius Kabi USA, LLC)
Medical deviceClass IReported June 10, 2026 · Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut... - UPC 22019700000 PAVILIONS CHOCOLATE COVERED STRAWBERRY 1 CT UPC 22117700000 recall (Albertsons Companies LLC)
FoodClass IIReported June 10, 2026 · Contains statement does not declare Hazelnut