Recalls affecting Alaska
Notices that name Alaska in their distribution area, plus every nationwide recall — nationwide recalls reach Alaska too.
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Class II · 3 months ago
Bell Pharmaceuticals, Inc Clinere, Carbamide Peroxide recall: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
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Class II · 3 months ago
Bell Pharmaceuticals, Inc QC Quality Choice, Carbamide Peroxide, 6.5% recall: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
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Class II · 3 months ago
Chiesi USA, Inc. Cleviprex 50 mg/100 mL , 10 Single Use Vials recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
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Class II · 3 months ago
Nutricia North America functional formularies Nourish Organic Whole Foods Meal recall: Subpotent for Vitamin A. The firm discovered that the testing laboratory used
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a…
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Class II · 3 months ago
Nutricia North America functional formularies Liquid Hope Organic Whole Foods Meal recall: Subpotent for Vitamin A. The firm discovered that the testing laboratory used
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a…
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NHTSA safety recall · 3 months ago
Ford Explorer and Lincoln Aviator recall: An unoccupied driver's seat may recline unintentionally during certain
An unoccupied driver's seat may recline unintentionally during certain scenarios, such as remote unlock or remote start.
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Highest risk · 3 months ago
Target Cat & Jack Children's Sandals recall: Risk of Serious Injury or Death from Choking Hazard
Risk of Serious Injury or Death from Choking Hazard
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Highest risk · 3 months ago
Panasonic Electric Toaster Ovens recall: Shock and Fire Hazards
Shock and Fire Hazards
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Highest risk · 3 months ago
Madewell Women's Sweaters recall: Due to Risk of Serious Injury or Death from Burn Hazard
Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Clothing Textiles
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Highest risk · 3 months ago
Huish Outdoors Hollis Diving Regulators recall: Risk of Serious Injury or Death from Drowning
Risk of Serious Injury or Death from Drowning
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Highest risk · 3 months ago
Currey & Company Nottaway Chandeliers recall: Risk of Serious Injury or Death from Electrocution Hazard
Risk of Serious Injury or Death from Electrocution Hazard
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NHTSA safety recall · 3 months ago
Nissan Armada, Infiniti QX56 and and 2014-2027 QX80 recall: The Gross Axle Weight Rating (GAWR) listed on the certification label
The Gross Axle Weight Rating (GAWR) listed on the certification label is incorrect, which can allow the vehicle to be overloaded. As such, these…
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Class II · 3 months ago
Integra LifeSciences Corp. OmniTract Surgical Retractor System recall: The current Omni-Tract Surgical Retractor System IFU states a dry time of 30
The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to…
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Class II · 3 months ago
Medline recall: Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots…
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Class II · 3 months ago
Medline recall: Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots…
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Class II · 3 months ago
Boston Scientific Neuromodulation Corporation Intracept Access Instruments recall: Intraosseous nerve ablation system instruments may have sterile barrier
Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility…
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Class II · 3 months ago
Think Surgical, Inc. Tmini Femur Tracking Array REF 109003 Udi-Di code: M9461090030 recall: Due to manufacturing/design issue where the knob on the tracking array
Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.
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Class II · 3 months ago
Elekta, Inc. Brand Name: Geneva Product Name: Brachytherapy Applicator recall: Due to safety concerns regarding the detachment of the tip
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
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Class II · 3 months ago
Elekta, Inc. Brand Name: Brachytherapy Applicator Product Name: Advanced recall: Due to safety concerns regarding the detachment of the tip
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
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Class II · 3 months ago
Fresenius Medical Care Holdings, Inc. 5008X Blood Tubing Set recall: Potential for Online Port Errors due to connection issues when connecting
Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the…
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Class II · 3 months ago
Elekta, Inc. Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name recall: Due to safety concerns regarding the detachment of the tip
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
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Class II · 3 months ago
Siemens Healthcare Diagnostics, Inc. Atellica CH Enzymatic Hemoglobin A1c . Material recall: The potential for intermittent well-to-well bias on the A1c_E assay
The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed…
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Class II · 3 months ago
Medline recall: Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots…
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Class II · 3 months ago
Cmr Surgical Limited Brand Name: Versius Surgical System US Product Name: Vesius recall: Secure Boot was mistakenly not enabled at manufacturing time
Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk.