Recalls affecting District of Columbia
Notices that name District of Columbia in their distribution area, plus every nationwide recall — nationwide recalls reach District of Columbia too.
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Class II · 1+ years ago
GE Medical Systems, LLC MAC VU360 Acquisition Trunk Cable and Module Holder recall: If a user incorrectly places the Acquisition Module into the Acquisition
If a user incorrectly places the Acquisition Module into the Acquisition Module Holder, it can result in excessive bending and wear of the…
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Class II · 1+ years ago
Synthes Products LLC LOW Prof Lckng Screw, F/IM Nail 5.0MM / L recall: Although the etched length on the screw is correct
Although the etched length on the screw is correct, the length marked on the external packaging is incorrect. Specifically, 42mm screws were packaged…
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Class I · 1+ years ago
ICU Medical, Inc. IV Administration sets. 23" 150 mL Burette Set w/Clave, Luer Lock recall: IV Gravity burette administration set burette component is missing
IV Gravity burette administration set burette component is missing an internal shutoff valve intended to stop fluid flow, which if used may result in…
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Class II · 1+ years ago
Becton Dickinson & Co. BD EpiCenter Microbiology Data Management System recall: Product service credentials used by some BD technical support teams to access
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these…
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Class II · 1+ years ago
Theken Companies LLC iNSitu Bipolar Hip System, Bipolar head implant Part ID recall: Downstream recall for RES 97605, BioPro femoral components. Product failed
Downstream recall for RES 97605, BioPro femoral components. Product failed transit testing. Impacted product may have potential issues with sterile…
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Class II · 1+ years ago
Cardinal Health 200, LLC Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 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
CPM Medical Consultants, LLC. Fuse ULTRA Foot Plating System Instructions for Use recall: Instructions for use for a foot plating system is being updated to remove
Instructions for use for a foot plating system is being updated to remove the second option of requirements for sterilization which was 3 minutes…
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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 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
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