Recalls in July 2026 (page 3)

416 recalls.

• Beckman Coulter DxC 500 AU Clinical Analyzer Modules using software version 1.5 or... recall (Beckman Coulter Inc.)
  Medical deviceClass IIReported August 26, 2026 · a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously modified by...
• Beckman Coulter DxC 500i Clinical Analyzer Modules using software version 1.5 or... recall (Beckman Coulter Inc.)
  Medical deviceClass IIReported August 26, 2026 · a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously modified by...
• Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev A recall (Paragon 28, Inc.)
  Medical deviceClass IIIReported August 26, 2026 · Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility.
• Custom Made Device Implant 6123 Navicular Cage Small Right Rev A recall (Paragon 28, Inc.)
  Medical deviceClass IIIReported August 26, 2026 · Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility.
• Blanketrol III recall (Gentherm Medical, LLC)
  Medical deviceClass IIReported August 26, 2026 · Overheating of the 115V CPU board may cause the device to shut down.
• Innercool Coolblue Console recall (Gentherm Medical, LLC)
  Medical deviceClass IIReported August 26, 2026 · Overheating of the 115V CPU board may cause the device to shut down.
• Blanketrol II Model 222S recall (Gentherm Medical, LLC)
  Medical deviceClass IIReported August 26, 2026 · Overheating of the 115V CPU board may cause the device to shut down.
• Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF#... recall (Paragonix Technologies Inc.)
  Medical deviceClass IIReported August 26, 2026 · Due to a firmware defect, the portable organ transfer device datalogger may lose its configuration, resulting in a blank screen and loss of displayed...
• Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF recall (Siemens Healthcare Diagnostics Products Ltd.)
  Medical deviceClass IIReported August 26, 2026 · Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.
• Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF:L2KSY2 recall (Siemens Healthcare Diagnostics Products Ltd.)
  Medical deviceClass IIReported August 26, 2026 · Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.
• Halyard LAVH PACK recall (AVID Medical, Inc.)
  Medical deviceClass IIReported August 26, 2026 · The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.
• Suture Cinch Long 1pk. Endoscopic tissue approximation device. recall (Boston Scientific Corporation)
  Medical deviceClass IIReported August 26, 2026 · Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.
• OverStitch Suture Cinch recall (Boston Scientific Corporation)
  Medical deviceClass IIReported August 26, 2026 · Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.
• TD Navio Maxi Speech Generating Device Model/Catalog Number: 1000799 recall (Tobii Dynavox Llc)
  Medical deviceClass IIReported August 26, 2026 · Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an...
• TD Navio Midi Speech Generating Device Model/Catalog Number: 1000798 recall (Tobii Dynavox Llc)
  Medical deviceClass IIReported August 26, 2026 · Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an...
• Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2... recall (Kico Knee Innovation Company)
  Medical deviceClass IIReported August 26, 2026 · Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing
• Cardiac Workstation 7000. Product Number: 860441. recall (Philips North America Llc)
  Medical deviceClass IIReported August 26, 2026 · Device will intermittently provide inaccurate data related to native heart rate.
• Cardiac Workstation 5000. Product Number: 860439. recall (Philips North America Llc)
  Medical deviceClass IIReported August 26, 2026 · Device will intermittently provide inaccurate data related to native heart rate.
• Dentsply Sirona Capsule Mixer Model No. 5546068 recall (SDI Limited)
  Medical deviceClass IIReported August 26, 2026 · Potential for electrical discharge from unit when unplugged.
• Ami HTX recall (Spectral Instruments Inc)
  Medical deviceClass IIReported August 26, 2026 · Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
• Lago X recall (Spectral Instruments Inc)
  Medical deviceClass IIReported August 26, 2026 · Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
• BD Needle Kit for Powered Driver 15mm x 15Ga recall (Bard Access Systems, Inc.)
  Medical deviceClass IReported August 26, 2026 · After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary...
• Cibus Fresh recall (Piazza Produce (dba CIBUS Fresh))
  FoodClass IReported August 19, 2026 · Possible Cyclospora Contamination
• TAYLOR FARMS BLEND LETT/ROM BLEND WITH BAG 4/5# Iceberg recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• MARKON BLEND LETT/ROM 80/20 WITH SEP BAGGIES 4/5# Iceberg recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• Cross Valley Farms BLEND LETT/ROM 80/20 WITH SEP BAGGIES 4/5# Iceberg recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• TAYLOR FARMS LETTUCE SALAD W/BAG 4/5# Iceberg recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• SYSCO LETTUCE SALAD MIX 4/5# SYSCO LETTUCE SALAD WITH SEP BAG 4/5# Iceberg recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• PEAK LETTUCE SALAD W/BAG 4/5# Iceberg recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• MARKON LETTUCE SALAD MIX 4/5# MARKON LETTUCE SALAD WITH SEP BAG 4/5# Iceberg recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• Cross Valley Farms LETTUCE SALAD MIX 4/5# Cross Valley Farms LETTUCE SALAD WITH SEP... recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• TAYLOR FARMS BLEND GARDEN SALAD MIX W/ROM 6/5# NATIONAL TAYLOR FARMS BLEND GARDEN... recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• SYSCO BLEND LETT/ROM 50/50 NOCLR 4/5# SYSCO BLEND LETT/ROM 70/30 NOCOLR 4/5# SYSCO... recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• MARKON BLEND LETT/ROM 50/50 NOCLR 4/5# MARKON BLEND LETT/ROM 80/20 4/5# Iceberg recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• Cross Valley Farms BLEND LETT/ROM 50/50 NOCLR 4/5# Cross Valley Farms BLEND LETT/ROM... recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• YUM LETTUCE SHREDDED 1/4" 6/5# Iceberg only products. recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• Jack in the Box 1/8" SHRED LETTUCE 4/5# Iceberg only products. recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• TAYLOR FARMS LETTUCE CHOP 1X1" 4/4# TAYLOR FARMS LETTUCE CHOP 1X1" 8/2# TAYLOR FARMS... recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• SYSCO LETTUCE CHOP 4/5# SYSCO LETTUCE SHRED 1/8" 4/5# Iceberg only products. recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• SUBWAY SHRED LETTUCE 1/4" 4/5# Iceberg only products. recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• PEAK LETTUCE SHRED 1/8" 4/5# Iceberg only products. recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• MARKON LETTUCE CHOP 4/5# MARKON LETTUCE SHRED 1/4" 4/5# MARKON LETTUCE SHRED 1/8" 4/5#... recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• MARKETSIDE ICEBERG SALAD 10/24 oz recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• Cross Valley Farms LETTUCE CHOP 4/5# Cross Valley Farms LETTUCE SHRED 1/4" 4/5# Cross... recall (Taylor Farms de Mexico S. de R.L. de C.V.)
  FoodClass IReported August 19, 2026 · Potential Cyclospora contamination.
• Aquafaba Powder recall (529 COMMERCE, LLC)
  FoodClass IReported August 19, 2026 · Undeclared Egg
• Grade A White In-shell Chicken eggs packaged in the following configurations: 1. Kroger recall (MIDWEST POULTRY SERVC C/O H & LELECTRIC)
  FoodClass IReported August 19, 2026 · Possible Salmonella Enteritidis
• Grade A Brown In-shell Chicken eggs packaged in the following configurations: 1. ... recall (MIDWEST POULTRY SERVC C/O H & LELECTRIC)
  FoodClass IReported August 19, 2026 · Possible Salmonella Enteritidis
• Honeyville YELLOW COLOR 1 GALLON NFI: WATER recall (FlavorsandColor.Com)
  FoodClass IIIReported August 19, 2026 · Undeclared Red #40.
• Vodka Tomato Sauce recall (SHEANDRO LLC)
  FoodClass IIReported August 19, 2026 · Label declares cream and cheese, but Milk is not declared
• Cefazolin in Dextrose recall (Baxter Healthcare Corporation)
  DrugClass IReported August 19, 2026 · Presence of Particulate Matter
• Optiray Imaging Bulk Package-350 recall (Liebel-Flarsheim Company LLC)
  DrugClass IReported August 19, 2026 · Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass.
• Glutathione recall (Victory Medical Center Pharmacy)
  DrugClass IReported August 19, 2026 · Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
• CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION recall (Heritage Pharmaceuticals Inc)
  DrugClass IIReported August 19, 2026 · Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles.
• CLEAR EYES Maximum Itchy Eye Relief recall (Prestige Brands Holdings)
  DrugClass IIReported August 19, 2026 · Lack of assurance of sterility. The recall is due to potential contamination
• SEMAGLUTIDE 20mg recall (Apollo Care, LLC)
  DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
• SEMAGLUTIDE 10mg recall (Apollo Care, LLC)
  DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
• SEMAGLUTIDE 7.5mg recall (Apollo Care, LLC)
  DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
• SEMAGLUTIDE 5mg recall (Apollo Care, LLC)
  DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
• SEMAGLUTIDE 2.5mg recall (Apollo Care, LLC)
  DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
• SEMAGLUTIDE 0.9mg recall (Apollo Care, LLC)
  DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
• SEMAGLUTIDE 9mg recall (Apollo Care, LLC)
  DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
• SEMAGLUTIDE 4.5mg recall (Apollo Care, LLC)
  DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
• SEMAGLUTIDE 6.75mg recall (Apollo Care, LLC)
  DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
• SEMAGLUTIDE 2.25MG recall (Apollo Care, LLC)
  DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
• SEMAGLUTIDE 12.5MG recall (Apollo Care, LLC)
  DrugClass IIReported August 19, 2026 · Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
• Cardinal Health Presource Kits: 1) BASIC PACK recall (Cardinal Health 200, LLC)
  Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
• Cardinal Health Presource Kits: 1) KIT recall (Cardinal Health 200, LLC)
  Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
• Cardinal Health Presource Kits: 1) CHI STD NEURO CRANI OPT 2 recall (Cardinal Health 200, LLC)
  Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
• Cardinal Health Presource Kits: 1) SEPTO RHINO PACK recall (Cardinal Health 200, LLC)
  Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
• Cardinal Health Presource Kits: 1) ENT TRAY recall (Cardinal Health 200, LLC)
  Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
• Cardinal Health Presource Kits: 1) NEWNAN SMR PACK recall (Cardinal Health 200, LLC)
  Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
• Cardinal Health Presource Kits: 1) HARMONIZED SPINE VCH PHC PACK recall (Cardinal Health 200, LLC)
  Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
• Cardinal Health Presource Kits: 1) FAT GRAFT ADD KIT recall (Cardinal Health 200, LLC)
  Medical deviceClass IIReported August 19, 2026 · Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
• Straumann Bone Level Tapered recall (Straumann USA LLC)
  Medical deviceClass IIReported August 19, 2026 · Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadvertently contain implants that are 12mm in length instead of 14mm as the...
• Endo-Model recall (Waldemar Link GmbH & Co. KG (Mfg Site))
  Medical deviceClass IIReported August 19, 2026 · The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a...
• OBP Medical recall (OBP Medical Corporation)
  Medical deviceClass IIReported August 19, 2026 · There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both...
• Philips Azurion recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported August 19, 2026 · Two software related issues: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate...
• Philips Azurion Rystem recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
  Medical deviceClass IIReported August 19, 2026 · Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural...
• GM Helix Implant recall (Straumann USA LLC)
  Medical deviceClass IIReported August 19, 2026 · There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the incorrect...
• Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL recall (Remel Europe Ltd.)
  Medical deviceClass IIReported August 19, 2026 · Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU criteria not positive to ATCC13102 within 60 Seconds.
• Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection recall (Spectra Medical Devices, Llc)
  Medical deviceClass IReported August 19, 2026 · Manufacturing firm, Huons, was cited for issues regarding product quality and sterility assurance. If the product sterility is compromised, patients may be...
• KC Everyday Mac & Cheese recall (Kerry, Inc)
  FoodClass IReported August 12, 2026 · Undeclared allergen (egg)
• Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree recall (PT Organics Limited)
  FoodClass IIReported August 12, 2026 · Possible foreign object (thin, soft plastic strands).
• Zen Principle Naturals Moringa Leaf Powder dietary supplement recall (FACTORY6, INC.)
  FoodClass IReported August 12, 2026 · Possible Salmonella in Moringa Leaf Powder product.
• Ultimate Mother's Day Wangshin Doenjang Aged 3 Years 9 oz. Korean Traditional Premium... recall (JINA F&C)
  FoodClass IIReported August 12, 2026 · Product label allergen "contains" statement does not include anchovy(fish)
• FLOUNDER SASHIMI WITH SAUCE recall (Eunha Fisheries Co., LTD)
  FoodClass IIReported August 12, 2026 · Foreign Manufacturer label contains Undeclared allergen ingredients Wheat, Soy, Sesame, Yellow #5 and Blue #1 in Frozen Flounder Products.
• Sliced Korean Halibut with Soy sauce recall (Eunha Fisheries Co., LTD)
  FoodClass IIReported August 12, 2026 · Foreign Manufacturer label contains Undeclared allergen ingredients Wheat, Soy, Sesame, Yellow #5 and Blue #1 in Frozen Flounder Products.
• Big Way Hot Pot "Hot Pot Miso Paste" recall (Big Way Ca Inc)
  FoodClass IIReported August 12, 2026 · Undeclared milk from lactose.
• "***Hondashi 0.25oz***" seasoning packed in silver plastic/metallic pouch recall (Pack'n Fresh LLC)
  FoodClass IIReported August 12, 2026 · Allergen missing from contains statement: fish
• Flexible food pouch recall (CHEER PACK)
  FoodClass IIReported August 12, 2026 · Flexible food pouch may release thin plastic strips into food.
• Spicy Breakfast Burrito sold under the following brand names: FRESH & READY FOODS... recall (M.G. Foods, Inc.)
  FoodClass IReported August 12, 2026 · Undeclared Soy. The firm received complaints of sausage in the burritos. Upon review the firm discovered the sausage contains soy which is not listed on the...
• Cyclophosphamide for Injection recall (Sunny Pharmtech Inc.)
  DrugClass IReported August 12, 2026 · Presence of Particulate Matter; identified as stainless steel
• Cyclophosphamide for Injection recall (Sunny Pharmtech Inc.)
  DrugClass IReported August 12, 2026 · Presence of Particulate Matter; identified as stainless steel
• Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag recall (Central Admixture Pharmacy Services Inc)
  DrugClass IIIReported August 12, 2026 · Incorrect Product Formulation
• Dicyclomine Hydrochloride Capsules recall (Aurobindo Pharma USA Inc)
  DrugClass IIReported August 12, 2026 · shortfill; reports of empty capsules.
• 5-PLASMA Bivalirudin Control recall (Aniara Diagnostica LLC)
  Medical deviceClass IIReported August 12, 2026 · Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of...
• 5-PLASMA Bivalirudin Calibrator recall (Aniara Diagnostica LLC)
  Medical deviceClass IIReported August 12, 2026 · Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of...
• 5-PLASMA Bivalirudin AMR Verification Kit recall (Aniara Diagnostica LLC)
  Medical deviceClass IIReported August 12, 2026 · Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of...
• Atellica CH Urine Albumin REF: 11537225 recall (Siemens Healthcare Diagnostics, Inc.)
  Medical deviceClass IIReported August 12, 2026 · Processing of urine albumin assay on the CI analyzers may lead to the following issues: Falsely depressed Atellica CH Urea Nitrogen (UN_c) results; Falsely...
• GE Healthcare Portrait Core Services SW V 1.2.0 recall (GE Medical Systems Information Technologies Inc)
  Medical deviceClass IIReported August 12, 2026 · A software vulnerability may allow unauthorized persons to gain privileged access to the device, which could result in loss of patient monitoring, missed...

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