Recalls affecting Minnesota
Notices that name Minnesota in their distribution area, plus every nationwide recall — nationwide recalls reach Minnesota too.
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Class II · 10 months ago
ICU Medical, Inc. LifeShield Drug Library Management recall: For certain customers, the Change Summary review option ceases to operate
For certain customers, the Change Summary review option ceases to operate as expected for any migrated library after the migration has been…
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Class II · 10 months ago
Zimmer, Inc. Brand Name: Affixus Antegrade Femoral Nailing System Product Name recall: Affected implants may have undersized distal diameter along length
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk…
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Class II · 10 months ago
Zimmer, Inc. Brand Name: Affixus Antegrade Femoral Nailing System Product Name recall: Affected implants may have undersized distal diameter along length
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk…
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Class II · 10 months ago
Medtronic Neuromodulation Restore Clinician Programmer Application recall: Software issue where a Device Reset message displayed on the app was unable
Software issue where a Device Reset message displayed on the app was unable to be cleared. In rare cases, this resulted in an inability to resume…
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Class II · 10 months ago
CareFusion 303, Inc. BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer recall: Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer
Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to…
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Class II · 10 months ago
Merck Sharp & Dohme LLC Noxafil Powdermix for Delayed-Release Oral Suspension, 300 mg recall: Presence of particulate matter: potential presence of metal particulates
Presence of particulate matter: potential presence of metal particulates in the product.
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Class II · 10 months ago
Merck Emend for oral suspension, 125 mg, Single-Dose Kit recall: Presence of particulate matter: potential presence of metal particulates
Presence of particulate matter: potential presence of metal particulates in the product.
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Class II · 10 months ago
A New Life Herbs, LLC Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea recall: Unapproved drug claims on product labeling and product misbranded
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
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Class II · 10 months ago
A New Life Herbs, LLC Baby Soothe Herbal Supplement, Promotes rest, helps ease colic recall: Unapproved drug claims on product labeling and product misbranded
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
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Class I · 10 months ago
Carousel Candies Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz recall: Undeclared pecan
Undeclared pecan
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Class II · 10 months ago
A New Life Herbs, LLC Boswellia Herbal Supplement, 1:5 Alcohol Double Extract recall: Unapproved drug claims on product labeling and product misbranded
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
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Class II · 10 months ago
A New Life Herbs, LLC Pain Away Herbal Supplement recall: Unapproved drug claims on product labeling and product misbranded
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
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Class II · 10 months ago
A New Life Herbs, LLC Ear Drops Herbal Supplement, Mullein flower alcohol tincture 1:5 recall: Unapproved drug claims on product labeling and product misbranded
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
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Class I · 10 months ago
Carousel Candies Choceur Pecan Cranberry & Cinnamon Holiday Bark. Standup Pouch Bag recall: Undeclared wheat
Undeclared wheat
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Class II · 10 months ago
A New Life Herbs, LLC Anti-virus Herbal Supplement, 1:5 Alcohol Tincture recall: Unapproved drug claims on product labeling and product misbranded
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
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Class II · 10 months ago
A New Life Herbs, LLC Sinus Cap Herbal Supplement, Herbs containing antibiotic recall: Unapproved drug claims on product labeling and product misbranded
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
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Class II · 10 months ago
A New Life Herbs, LLC Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract recall: Unapproved drug claims on product labeling and product misbranded
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
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Class II · 10 months ago
A New Life Herbs, LLC Organic Ginger Root Herbal Supplement, Natural anti-inflammatory recall: Unapproved drug claims on product labeling and product misbranded
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
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Class II · 10 months ago
Chips Ahoy Baked brownie bites recall: Product Safety – choking threats
Product Safety – choking threats
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Class II · 10 months ago
Gold Star Distribution All FDA-regulated products held at facility including drugs recall: Potential Salmonella contamination, presence of rodent and avian
Potential Salmonella contamination, presence of rodent and avian contamination and insanitary conditions during the storage process.
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Class I · 10 months ago
GE Medical Systems China Co., Ltd. GE Healthcare Carestation anesthesia system Power recall: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power…
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Class II · 10 months ago
Dsaart LLC Brand Name: AART Gluteal Implant Product Name: Gluteal Implant recall: Due to manufactured products that deviated from established specifications
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket…
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Class II · 10 months ago
Dsaart LLC Brand Name: AART Pectoral Implant Product Name: Pectoral Implant Model/ recall: Due to manufactured products that deviated from established specifications
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket…
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Class II · 10 months ago
DICOM Grid, Inc. Intelerad InteleShare software, with ProViewer component recall: Software intended to aid in diagnosing conditions
Software intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are…