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 · 12 months ago
Total Joint Orthopedics, Inc. Brand Name: Klassic BiPolar Head Model/ recall: Potential packaging issue that could compromise the sterile barrier. Defect
Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk…
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Class II · 12 months ago
B-K Medical A/S UUltrasound System 2300, bkActiv w/battery recall: GE HealthCare has become aware that the Instructions for Use within the user
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery…
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Class II · 12 months ago
Mozarc Medical US LLC Mahurkar" Acute High Pressure Triple Lumen Catheter Tray Curved recall: A potential issue with the seal integrity of header bag packaging
A potential issue with the seal integrity of header bag packaging.
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Class II · 12 months ago
B-K Medical A/S bk5000 Ultrasound System w/battery recall: GE HealthCare has become aware that the Instructions for Use within the user
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery…
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Class II · 12 months ago
B-K Medical A/S Ultrasound System 1300, bkSpecto w/battery recall: GE HealthCare has become aware that the Instructions for Use within the user
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery…
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Class II · 12 months ago
Mozarc Medical US LLC Mahurkar" Acute High Pressure Triple Lumen Catheter Tray recall: A potential issue with the seal integrity of header bag packaging
A potential issue with the seal integrity of header bag packaging.
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Class I · 12 months ago
Integra LifeSciences Corp. Codman Disposable Perforator 11mm. Cranial Perforator recall: Expansion of recall of size 14 mm Codman Disposable Perforators
Expansion of recall of size 14 mm Codman Disposable Perforators for inadequate welds to size 11 mm and 9 mm Codman Disposable Perforators out of an…
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Class II · 12 months ago
Mozarc Medical US LLC Mahurkar" Acute High Pressure Triple Lumen Catheter Tray Curved recall: A potential issue with the seal integrity of header bag packaging
A potential issue with the seal integrity of header bag packaging.
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Class II · 12 months ago
Zydus Pharmaceuticals Inc clomiPramine Hydrochloride, Capsules, USP, 75 mg recall: cGMP deviations: an observed Out of Specification of Nitrosamine Drug
cGMP deviations: an observed Out of Specification of Nitrosamine Drug Substance-Related Impurities (NDSRIs), N-Nitroso Desmethyl-Clomipramine, above…
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Class II · 12 months ago
Zydus Pharmaceuticals Inc clomiPramine Hydrochloride, Capsules, USP, 50 mg recall: cGMP deviations: an observed Out of Specification of Nitrosamine Drug
cGMP deviations: an observed Out of Specification of Nitrosamine Drug Substance-Related Impurities (NDSRIs), N-Nitroso Desmethyl-Clomipramine, above…
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Class II · 12 months ago
Zydus Pharmaceuticals Inc clomiPramine Hydrochloride, Capsules, USP, 25 mg recall: cGMP deviations: an observed Out of Specification of Nitrosamine Drug
cGMP deviations: an observed Out of Specification of Nitrosamine Drug Substance-Related Impurities (NDSRIs), N-Nitroso Desmethyl-Clomipramine, above…
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Class II · 12 months ago
Aero Healthcare Acetaminophen 500mg Caffeine 65mg caplets recall: Labeling: Label Mix-up. This issue affects the outer box labeling only
Labeling: Label Mix-up. This issue affects the outer box labeling only. The box incorrectly states the ingredients Acetaminophen 500mg and Caffeine…
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Class I · 12 months ago
ByHeart Whole Nutrition Infant formula 24 oz cans and 0.6oz packets recall: Potential Foodborne Illness – Clostridium botulinum
Potential Foodborne Illness – Clostridium botulinum
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Highest risk · 12 months ago
Moonlight/Kroger Yellow and white peaches recall: Potential to be contaminated with Listeria monocytogenes
Potential to be contaminated with Listeria monocytogenes.
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Class I · 12 months ago
Fresenius Kabi Famotidine Injection, USP 20 mg per 2 mL recall: Out-of-specification endotoxin results
Out-of-specification endotoxin results
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NHTSA safety recall · 12 months ago
Chrysler Jeep Grand Cherokee 4XE and Jeep Wrangler 4XE Plug-In Hybrid recall: Debris inside the engine may cause engine failure
Debris inside the engine may cause engine failure, which can result in a loss of drive power and/or an engine compartment fire.
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Elevated risk · 12 months ago
Three-Wheeled Children's Scooter with Foot Brake recall: The left front wheel can detach during use, posing a fall hazard
The left front wheel can detach during use, posing a fall hazard.
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Highest risk · 12 months ago
Stihl BR 800 Backpack Blowers recall: Laceration Hazard
Laceration Hazard
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Elevated risk · 12 months ago
Peloton Original Series Bike+ Exercise Bikes recall: Fall and Injury Hazards
Fall and Injury Hazards
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Highest risk · 12 months ago
Lezyne USA Bicycle Floor Pumps recall: Serious Injury Hazard
Serious Injury Hazard
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Highest risk · 12 months ago
Inkari Plush Alpaca Toys recall: The recalled toys are intended for children under three years of age
The recalled toys are intended for children under three years of age and the eyes can detach, which violates the small parts ban, posing a choking…
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Class II · 12 months ago
CareFusion 303, Inc. Various models of BD Pyxis Medbank: Reference numbers: 1137-00 recall: Potential fluid ingress of anesthesia station or med station may result
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
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Class II · 12 months ago
CareFusion 303, Inc. All Serial Numbers/BD Pyxis CII Safe ES Tower Main, REF: 1116-00 recall: Potential fluid ingress of anesthesia station or med station may result
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
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Class II · 12 months ago
Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices recall: Due to incomplete seals in the pouch which provide the sterile barrier
Due to incomplete seals in the pouch which provide the sterile barrier.