Recalls affecting Virginia
Notices that name Virginia in their distribution area, plus every nationwide recall — nationwide recalls reach Virginia too.
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Class II · 1+ years ago
Cardinal Health 200, LLC Salem Sump PVC Tubes: Product Code/Product Name: 264929 recall: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for…
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Class II · 1+ years ago
Cardinal Health 200, LLC Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 recall: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for…
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Class II · 1+ years ago
Baxter Healthcare Corporation Oral Probe , accessory used with Welch Allyn SureTemp recall: Affected oral/axillary probes were inadvertently programmed with the rectal
Affected oral/axillary probes were inadvertently programmed with the rectal probe configuration. Affected probes will potentially display a lower…
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Class II · 1+ years ago
Medline Industries, LP Excelsior Medical, 0.9% Sodium Chloride Injection recall: Medline has identified a limited quantity of saline IV flush syringes
Medline has identified a limited quantity of saline IV flush syringes that may not meet the required concentration of sodium chloride.
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Class II · 1+ years ago
Bristol-Myers Squibb Company Opdualag injection, 240 mg and 80 mg/20 mL recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility.
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Class II · 1+ years ago
Aspiro Pharma Limited Ketorolac Tromethamine Injection, USP, 60 mg/2 mL recall: Presence of Particulate Matter: Particulate matter identified as glass
Presence of Particulate Matter: Particulate matter identified as glass
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Class II · 1+ years ago
Church & Dwight Co., Inc. Zicam" Medicated Fruit Drops Elderberry Flavor recall: Labeling: Label Mix-up: The product in the bottle contains elderberry
Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.
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Class III · 1+ years ago
JB Chemicals and Pharmaceuticals Ltd Cetirizine Hydrochloride Tablets USP 10 mg recall: Tablet/Capsules Imprinted with Wrong ID
Tablet/Capsules Imprinted with Wrong ID
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Class II · 1+ years ago
The Harvard Drug Group LLC Gabapentin Capsules, USP, 100 mg, 100 Capsules recall: Failed Impurities/Degradation Specifications: an out of specification result
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
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Class II · 1+ years ago
Medline, Alcohol Prep Pads , 100 eaches per box recall: Subpotent Drug
Subpotent Drug
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Class II · 1+ years ago
USV Private Limited Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 % recall: Failed Impurities/Degradation Specifications: The result for 'Any individual
Failed Impurities/Degradation Specifications: The result for 'Any individual unspecified impurity' exceeds the specification limit.
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Class II · 1+ years ago
ibspot Taoscare Motion Sickness Patches 36-count box recall: Marketed Without an Approved NDA/ANDA
Marketed Without an Approved NDA/ANDA
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Class III · 1+ years ago
JB Chemicals and Pharmaceuticals Ltd Cetirizine Hydrochloride Tablets USP 10 mg recall: Tablet/Capsules Imprinted with Wrong ID
Tablet/Capsules Imprinted with Wrong ID
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Class II · 1+ years ago
The Harvard Drug Group LLC Gabapentin Capsules, USP, 100 mg, 10 Capsules recall: Failed Impurities/Degradation Specifications: an out of specification result
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
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Class II · 1+ years ago
Lannett Company Inc. Niacin Extended-release Tablets, USP, 1,000 mg recall: Failed Dissolution Specifications
Failed Dissolution Specifications
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Class II · 1+ years ago
Graviti Pharmaceuticals Private Limited Bupropion Hydrochloride Extended-Release recall: Failed Tablet/Capsule Specifications
Failed Tablet/Capsule Specifications
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Class I · 1+ years ago
M.C.I. Foods, Inc. Cheese and Egg with Green Salsa Breakfast Burrito recall: Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
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Class I · 1+ years ago
Wegmans Brulee Cheesecake Large recall: Contains undeclared pecans
Contains undeclared pecans
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Class I · 1+ years ago
Wegmans Food Markets, Inc. Large Ultimate Fresh Fruit Topped Cheesecake recall: Contains undeclared pecans
Contains undeclared pecans
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Class I · 1+ years ago
Turkana Food Inc. Floria Dried Apricots, 200 Gram packages, 40 packages per case recall: Product contains undeclared sulfites
Product contains undeclared sulfites.
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Class I · 1+ years ago
Wegmans Large Ultimate Strawberry Topped Cheesecake recall: Contains undeclared pecans
Contains undeclared pecans
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Class I · 1+ years ago
Wegmans Large Ultimate Cherry Topped Cheesecake recall: Contains undeclared pecans
Contains undeclared pecans
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Class I · 1+ years ago
Wegmans Large Ultimate Plain Cheesecake recall: Contains undeclared pecans
Contains undeclared pecans
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Class I · 1+ years ago
M.C.I. Foods, Inc. Egg and Cheese Breakfast Burrito recall: Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes