Recalls in Alabama (page 11)

3952 recalls.

• Nitroglycerin injection recall (American Regent, Inc.)
  DrugClass IIReported August 26, 2026 · Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
• Morphine Sulfate Injection recall (Fresenius Kabi USA, LLC)
  DrugClass IReported August 26, 2026 · Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL.
• Acamprosate Calcium recall (Mylan Pharmaceuticals Inc)
  DrugClass IIReported August 26, 2026 · Failed Dissolution Specifications
• Carbamazepine Tablets recall (Golden State Medical Supply Inc.)
  DrugClass IIReported August 26, 2026 · CGMP deviations: tablets with black specks.
• Carbamazepine Tablets recall (SUN PHARMACEUTICAL INDUSTRIES INC)
  DrugClass IIReported August 26, 2026 · CGMP Deviations; black spots found on tablets from burnt excipient during manufacturing
• Libtayo recall (Regeneron Pharmaceuticals Inc)
  DrugClass IIReported August 26, 2026 · Lack of Assurance of Sterility
• PEMRYDI RTU recall (Shilpa Medicare Limited)
  DrugClass IIReported August 26, 2026 · Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
• PEMRYDI RTU recall (Shilpa Medicare Limited)
  DrugClass IIReported August 26, 2026 · Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
• Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard... recall (restor3d Inc.)
  Medical deviceClass IIReported August 26, 2026 · Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws.
• Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703 recall (ConvaTec, Inc)
  Medical deviceClass IIReported August 26, 2026 · Urostomy Pouches may leak from cap during use.
• Fort Defiance Industries recall (Fort Defiance Industries, LLC)
  Medical deviceClass IIReported August 26, 2026 · The Automated Field Steam Sterilizer's water recovery system 120V Amphenol connector may experience an intermittent loss of ground continuity, which could...
• Boston Scientific ENROUTE Transcarotid Neuroprotection System Plus recall (Boston Scientific Corporation)
  Medical deviceClass IReported August 26, 2026 · Potential for arterial sheath tip separation or partial tip separation during use.
• Boston Scientific ENROUTE Transcarotid Neuroprotection System recall (Boston Scientific Corporation)
  Medical deviceClass IReported August 26, 2026 · Potential for arterial sheath tip separation or partial tip separation during use.
• Beckman Coulter recall (Siemens Healthcare Diagnostics, Inc.)
  Medical deviceClass IIReported August 26, 2026 · Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine...
• Syva EMIT 2000 Quinidine Assay REF: 4Q019UL Contents: 1x28 mL recall (Siemens Healthcare Diagnostics, Inc.)
  Medical deviceClass IIReported August 26, 2026 · Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine...
• 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.
• 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.
• GETINGE Y SENSOR Module recall (Maquet Critical Care AB)
  Medical deviceClass IIReported August 26, 2026 · The module did not undergo electrical safety tests and functional tests during production.
• 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...
• Arrow-LOK Implant recall (Arrowhead DE LLC)
  Medical deviceClass IIReported August 26, 2026 · Implant did not undergo required gamma radiation dose audit. A potential reduction in sterility assurance could lead to patient infection.
• 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.
• One-Piece Guedel Airway recall (Intersurgical Inc)
  Medical deviceClass IIReported August 26, 2026 · Devices could potentially be occluded or partially occluded.
• One-Piece Guedel Airway recall (Intersurgical Inc)
  Medical deviceClass IIReported August 26, 2026 · Devices could potentially be occluded or partially occluded.
• Hamilton Microlab STAR Liquid Handler recall (Foundation Medicine, Inc.)
  Medical deviceClass IIReported August 26, 2026 · Software issue that can cause an increase in spontaneous software closures.
• EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 ... recall (Covidien, LLC)
  Medical deviceClass IIReported August 26, 2026 · The system's 24-hour usage limit results in catheters incorrectly flagged as expired, making them unavailable for clinical procedures.
• CCM Hockey U.S. Recalls FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories Due to Risk of Injury from Laceration or Impact Hazards
  Consumer productReported August 20, 2026 · The recalled hockey visors and replacement visor accessories can crack upon impact, posing a risk of injury due to laceration or impact hazards.
• Workbless Pressure Washers Recalled Due to Risk of Serious Injury or Death from Shock and Electrocution Hazards
  Consumer productReported August 20, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing serious risks of injury or...
• Koorlian Mattresses Recalled Due to Risk of Serious Injury or Death from Fire Hazard; Violate Mandatory Standard for Mattress Flammability; Sold on Amazon by Dream Bedding Technology
  Consumer productReported August 20, 2026 · The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire.
• JINHEZO Mini Waterproof LED Tea Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries; Imported by Mystic ZO
  Consumer productReported August 20, 2026 · The LED Tea Lights violate the mandatory safety standard for consumer products with button cell and coin batteries because the button batteries can be accessed...
• Goal Zero Recalls YETI 3000X Power Stations Due to Serious Risk of Injury from Fire and Burn Hazards
  Consumer productReported August 20, 2026 · The recalled power station's circuit board can overheat, posing a risk of serious injury from fire and burn hazards.
• Modine Manufacturing Company Recalls Airedale Heating and Cooling Ventilation Fans Due to Fire Hazard
  Consumer productReported August 20, 2026 · The ventilation fan motor in the heat pumps can short circuit if water gets on the circuit board, causing the units to overheat and posing a fire hazard.
• KTM North America Recalls Off-Road Motorcycles Due to Risk of Serious Injury or Death from Crash Hazard
  Consumer productReported August 20, 2026 · The rear brake caliper can crack or break, reducing the brake system's effectiveness, posing a risk of serious injury or death due to crash hazard.
• 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.
• ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000 recall (Erbe USA Inc)
  Medical deviceClass IIReported August 19, 2026 · A strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumatic short circuit between he gas inlet and the connector resulting in...
• BIOFIRE Respiratory Panel 2.1 recall (BioFire Diagnostics, LLC)
  Medical deviceClass IIReported August 19, 2026 · Due to increase in false negative results
• 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...
• 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...
• Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 ... recall (Spacelabs Healthcare, Inc.)
  Medical deviceClass IIReported August 19, 2026 · Due to off-the-shelf display port component that has audio/video failures
• navify Digital Pathology recall (Ventana Medical Systems, Inc.)
  Medical deviceClass IIReported August 19, 2026 · Due to complaints received for the Image Management System regarding image/metadata discrepancy with the Viewer window
• BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL ... recall (MICROVENTION INC.)
  Medical deviceClass IIReported August 19, 2026 · Due to an increase rate of balloon pinhole defects.
• 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
• SILDENAFIL CITRATE USP recall (Shoolin Pharma Chem LLP)
  DrugClass IIReported August 19, 2026 · CGMP Deviations:Noted during FDA inspection
• TADALAFIL USP recall (Shoolin Pharma Chem LLP)
  DrugClass IIReported August 19, 2026 · CGMP Deviations:Noted during FDA inspection
• TADALAFIL USP recall (Shoolin Pharma Chem LLP)
  DrugClass IIReported August 19, 2026 · CGMP Deviations:Noted during FDA inspection
• TADALAFIL USP recall (Shoolin Pharma Chem LLP)
  DrugClass IIReported August 19, 2026 · CGMP Deviations:Noted during FDA inspection
• SILDENAFIL CITRATE USP recall (Shoolin Pharma Chem LLP)
  DrugClass IIReported August 19, 2026 · CGMP Deviations:Noted during FDA inspection
• 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
• Diovan recall (Novartis Pharmaceuticals Corporation)
  DrugClass IIReported August 19, 2026 · Failed Dissolution Specifications
• 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.

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