Recalls affecting Oregon
Notices that name Oregon in their distribution area, plus every nationwide recall — nationwide recalls reach Oregon too.
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Class II · 4 months ago
Micromed S.p.A. SD LTM 64 PLUS, EEG Amplifier/recorder, Model/ recall: Natus has become aware of two complaints related to the SD LTM 64 PLUS where
Natus has become aware of two complaints related to the SD LTM 64 PLUS where the EEG traces acquired from two or four different amplifiers used in a…
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Class II · 4 months ago
Boston Scientific CSK Electrodes: REF: Csk-Tc10 recall: Reusable electrodes may not meet expected performance levels
Reusable electrodes may not meet expected performance levels.
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Class II · 4 months ago
INSPIREMD Inc Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/ recall: Stent delivery system may encounter complications during deployment
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
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Class II · 4 months ago
Avanos Medical, Inc. Brand Name: Corflo Product Name: Corflo Safety PEG Kit Model/ recall: Lidocaine hydrochloride injection, the subject of a supplier recall
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
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Class II · 4 months ago
Avanos Medical, Inc. Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG recall: Lidocaine hydrochloride injection, the subject of a supplier recall
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
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Class II · 4 months ago
Avanos Medical, Inc. Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG recall: Lidocaine hydrochloride injection, the subject of a supplier recall
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
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Class II · 4 months ago
Mozarc Medical US LLC Mahurkar Elite PASS Trays recall: The Tegaderm CHG dressing, as specified in product labeling
The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays.
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Class II · 4 months ago
Avanos Medical, Inc. Product Name: Corflo* Safety PEG Kit with ENFit¿ Connector Model/ recall: Lidocaine hydrochloride injection, the subject of a supplier recall
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
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Class II · 4 months ago
Avanos Medical, Inc. Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG recall: Lidocaine hydrochloride injection, the subject of a supplier recall
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
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Class II · 4 months ago
Avanos Medical, Inc. Product Name: Corflo* Safety PEG Kit with ENFit¿ Connector Model/ recall: Lidocaine hydrochloride injection, the subject of a supplier recall
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
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Class II · 4 months ago
GE Medical Systems, LLC Allia IGS 3 Pulse angiographic X-ray system recall: GE HealthCare has become aware of a potential issue affecting an electrical
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue…
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Class II · 4 months ago
INSPIREMD Inc Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/ recall: Stent delivery system may encounter complications during deployment
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
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Class III · 4 months ago
Amneal Pharmaceuticals, LLC Primidone Tablets, USP, 50 mg, 100 Tablets per Bottle recall: Cross Contamination with Other Products: due to a potential
Cross Contamination with Other Products: due to a potential for cross-contamination with Acemetacin API due to an issue at the API manufacturer.
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Class II · 4 months ago
Breckenridge Pharmaceutical, Inc. Duloxetine Delayed-Release Capsules, USP recall: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
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Class III · 4 months ago
Fresenius Kabi USA, LLC Epinephrine Injection, USP, 1mg/mL, 1 mL single-dose vial recall: Failed Impurities/Degradations Specifications
Failed Impurities/Degradations Specifications
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Class II · 4 months ago
Breckenridge Pharmaceutical, Inc. Duloxetine Delayed-Release Capsules, USP, 60mg recall: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
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Class II · 4 months ago
Zep, Alcohol Sanitizer Spray, Ethanol 70% recall: Microbial contamination of sterile products
Microbial contamination of sterile products
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Class II · 4 months ago
Sun Pharmaceutical Industries Inc Budesonide Inhalation Suspension, 1mg/2mL recall: Presence of Foreign Substance:This recall has been initiated in response
Presence of Foreign Substance:This recall has been initiated in response to a product quality complaint reported for black/brown specs and particles…
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Class II · 4 months ago
Ascend Laboratories, LLC Minocycline Hydrochloride Extended-Release Tablets, USP recall: Failed Dissolution Specifications: An out-of-specification (OOS) result
Failed Dissolution Specifications: An out-of-specification (OOS) result was observed during the 9th month of dissolution test analysis
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Class II · 4 months ago
Sensory Supplement LLC Neuro Nourish dietary supplement recall: Premature lipid oxidation causing quality issue potentially causing product
Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.
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Class II · 4 months ago
BEF Foods, Inc Park St. Deli Macaroni & Cheese recall: Undeclared allergen (soy lecithin)
Undeclared allergen (soy lecithin).
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Class II · 4 months ago
U.S. Trading Company Dragonfly Thai Ginger Powder Net Weight: 4.37 oz Product recall: Potential contamination with lead
Potential contamination with lead.
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Class III · 4 months ago
Wild Coast Brew LLC The Shadow Loose-Leaf Tea - Winter Spice Black Tea recall: Dry tea blends product containing Ashwagandha root which is an unsafe food
Dry tea blends product containing Ashwagandha root which is an unsafe food additive.
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Class III · 4 months ago
Wild Coast Brew LLC The Creator Loose-Leaf Tea - Ginger Lemongrass Tisane recall: Dry tea blends product containing Ashwagandha root which is an unsafe food
Dry tea blends product containing Ashwagandha root which is an unsafe food additive.