foundmatterdb

Field reports on stuff that let you down

Medications

487 reports

FDA recallMedicationsClass II· Par Health USA, LLC

Buprenorphine Hydrochloride, Injection 0.3 mg/mL, Rx Only, 5 x 1 mL Single Dose Vials, Manufactured for: Endo USA, Malvern, PA, NDC 42023-179-05 Reason: Crystallization Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · U.S. Nationwide

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FDA recallMedicationsClass II· Ajanta Pharma USA Inc

Ranolazine Extended-Release Tablets, 1000 mg, 60-count bottle, Rx Only, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807. NDC: 27241-126-02 Reason: Failed Dissolution Specifications: below specification Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · Nationwide in the US.

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Official feedMedications· FDA MedWatch safety alerts

Nova Biomedical® Announces Global Medical Device Correction for StatStrip® Glucose Hospital Meter WALTHAM, Mass., October 5, 2026 – Nova Biomedical initiated a global Medical Device Correction on July 24, 2026, for the StatStrip® Glucose Hospital Meter System due to a software issue that may cause a glucose result to be associated with the wrong patient. Wh…

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FDA drug shortageMedications· Amneal Pharmaceuticals

Shortage: Methylprednisolone Acetate Injection — Methylprednisolone Acetate, Injection, 80 mg/1 mL (NDC 70121-1574-5) Status: Current Used for: Rheumatology

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FDA drug shortageMedications· InfoRLife SA

Shortage: Ropivacaine Hydrochloride Injection — Ropivacaine Hydrochloride, Injection, 2 mg/1 mL (NDC 25021-671-87) Status: Current Used for: Anesthesia

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Official feedMedications· FDA MedWatch safety alerts

IV Tubing Set Correction: ICU Medical Updates Use Instructions for IV Tubing Sets Black specks and particulate reported in drip chambers of certain ICU Medical IV tubing sets does not affect device safety, performance, or intended use.

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Official feedMedications· FDA MedWatch safety alerts

Breathing Circuit RecallThe maker or a government agency pulled this product. Check the model or lot number and stop using it until it's fixed or refunded.: Draeger Removes VentStar Resus Neo Hoses Removal of VentStar Resus Neo hoses due to the potential for cracks resulting in restricted ventilation or delayed therapy.

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FDA drug shortageMedications· Aurobindo Pharma USA

Shortage: Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate Tablet — Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 3.75 mg; 3.75 mg; 3.75 mg; 3.75 mg (NDC 13107-072-01) Status: Current Reason: Shortage of an active ingredi…

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FDA drug shortageMedications· Aurobindo Pharma USA

Shortage: Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate Tablet — Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 5 mg; 5 mg; 5 mg; 5 mg (NDC 13107-073-01) Status: Current Reason: Shortage of an active ingredient Used for…

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FDA drug shortageMedications· Aurobindo Pharma USA

Shortage: Clonazepam Tablet — Clonazepam, Tablet, .5 mg (NDC 59651-722-01) Status: Current Used for: Neurology, Pediatric, Psychiatry

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FDA drug shortageMedications· Aurobindo Pharma USA

Shortage: Quinapril Hydrochloride Tablet — Quinapril Hydrochloride, Tablet, 10 mg (NDC 65862-618-90) Status: Current Reason: Discontinuation of the manufacture of the drug Used for: Cardiovascular

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FDA drug shortageMedications· Aurobindo Pharma USA

Shortage: Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate Tablet — Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 1.25 mg; 1.25 mg; 1.25 mg; 1.25 mg (NDC 13107-068-01) Status: Current Reason: Shortage of an active ingredi…

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Official feedMedications· FDA MedWatch safety alerts

Greenwich Rx Issues Voluntary Nationwide RecallThe maker or a government agency pulled this product. Check the model or lot number and stop using it until it's fixed or refunded. of Compounded Glutathione Due to Elevated Endotoxin Levels IMMEDIATE RELEASE - Tomball, Texas – October 1, 2026 – Greenwich Rx, a 503A compounding pharmacy, is voluntarily recalling specific lots of its compounded glutathione to the consumer level. The product is being recalled due to potential elevated endoto…

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FDA drug shortageMedications· HQ Specialty Pharma

Shortage: Dexmedetomidine Hydrochloride Injection — Dexmedetomidine Hydrochloride, Injection, 4 ug/1 mL (NDC 44567-602-24) Status: Current Used for: Anesthesia

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FDA drug shortageMedications· WG Critical Care

Shortage: Midazolam Hydrochloride Injection — Midazolam In 0.9% Sodium Chloride, Injection, 1 mg/1 mL (NDC 44567-610-10) Status: Current Used for: Anesthesia, Neurology

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FDA recallMedicationseye dropAlternatives →Class II· Sterling Pharmaceutical Services LLC

TRP The Relief Products* Gentle Eyes Lubricant Eye Drops18 reports about eye drop on this site. See them all →, Carboxymethylcellulose sodium 0.5%, Sterile Eye Drops, 0.5 FL OZ (15 mL) bottles, Manufactured exclusively for TRP Company, Inc. 1575 Delucci Ln, Reno, NV 89502, NDC 17312-430-15. Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

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FDA recallMedicationseye dropAlternatives →Class II· Sterling Pharmaceutical Services LLC

AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Lubricant Eye Drops18 reports about eye drop on this site. See them all →, Sterile, 0.5 FL OZ (15 mL) EACH, 1.0 FL OZ (30 mL) TOTAL, 2 count Twin Pack, Distributed by: AVKARE, Pulaski, TN, 38478, NDC 50268-068-02 (carton) Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

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FDA recallMedicationseye dropAlternatives →Class II· Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare…

Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops18 reports about eye drop on this site. See them all → (glycerin 0.25%, naphazoline hydrochloride 0.012%) with Hang Tag, 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15 Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · Nationwide in the USA.

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FDA recallMedicationseye dropAlternatives →Class II· Sterling Pharmaceutical Services LLC

AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Lubricant Eye Drops18 reports about eye drop on this site. See them all →, Sterile, 0.5 FL OZ (15 mL) bottle, Distributed by: AVKARE, Pulaski, TN, 38478, NDC 50268-068-15 Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

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FDA recallMedicationseye dropAlternatives →Class II· Sterling Pharmaceutical Services LLC

Lubricant Eye Drops18 reports about eye drop on this site. See them all →-Cameron Pharmaceuticals, Carboxymethylcellulose Sodium 0.5%, Eye Lubricant, 0.5 FL OZ (15 mL) bottles, Distributed by Cameron Pharmaceuticals, LLC, Louisville, KY, 40245, NDC 42494-448-05 Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

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FDA recallMedicationsClass II· Sterling Pharmaceutical Services LLC

Reliable -1 Laboratories, Sodium Chloride Hypertonicity Ophthalmic Solution, 5%, Sterile, 0.5 FL OZ (15 mL) bottles, Distributed by: Reliable-1 Laboratories LLC, Valley Stream, NY, 11580, NDC 69618-077-55. Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

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FDA recallMedicationseye dropAlternatives →Class II· Sterling Pharmaceutical Services LLC

Walgreens Lubricant Eye Drops18 reports about eye drop on this site. See them all →, 0.5 FL OZ (15 mL) 1.0 FL OZ (30 mL) TOTAL, 2 count Twin Pack, Distributed by Walgreens Co., 200 Wilmot Road, Deerfield, IL 60015, NDC 0363-8833-15. Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

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FDA recallMedicationsClass II· Amneal Pharmaceuticals of New York, LLC

Exenatide Injection, USP, 250 mcg/mL, 1.2 mL per prefilled pen, Rx Only, Subcutaneous Use Only, For Single Patient Use Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad 382213, India; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 70121-1685-1 Reason: Defective Delivery System: Possibility of no medication in the pre…

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FDA recallMedicationsClass III· Macleods Pharmaceuticals Limited

Olanzapine Tablets, USP 5 mg, 30-count bottle, Rx Only, Manufactured For: Macleods Pharma USA, Inc. Princeton, NJ, 08540; Manufactured by: Macleods Pharmaceuticals, Ltd, Baddi, Himachal Pradesh, INDIA, NDC 33342-068-07. Reason: Failed Impurities/Degradation Specifications:Organic and unspecified impurities above specification. Class IIIThe lowest FDA recall level: unlikely to cause health problems, but it breaks the rules. · Ongoing · Nationwi…

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FDA recallMedicationsointmentAlternatives →Class II· Sterling Pharmaceutical Services LLC

Major LubriFresh P.M. Nighttime Ointment3 reports about ointment on this site. See them all →, Net wt. 0.125 oz. (3.5 g) tubes, Distributed by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152, NDC 0904-6488-38 Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

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FDA recallMedicationseye dropAlternatives →Class II· Sterling Pharmaceutical Services LLC

Walgreens Lubricant Eye Drops18 reports about eye drop on this site. See them all →, Carboxymethylcellulose sodium 0.5%, Lubricant Eye Drops, Sterile, 0.5 OZ (15 mL) bottles, Distributed by Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-8833-15. Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

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FDA recallMedicationseye dropAlternatives →Class II· Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare…

Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops18 reports about eye drop on this site. See them all → (glycerin 0.25%, naphazoline hydrochloride 0.012%) , 0.5 fl oz (15mL) per dropper bottle, STERILE, Dist. by Medtech Products Inc., Tarrytown, NY 10591. NDC: 67172-797-15 Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · Nationwide in the USA.

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FDA recallMedicationsClass II· Sterling Pharmaceutical Services LLC

Reliable-1 Laboratories Lubricating Tears, Sterile, 0.5 FL OZ (15 mL) bottles, Distributed by: Reliable-1 Laboratories LLC, Valley Stream, NY, 11580, www.reliable1labs.com, NDC 69618-076-55. Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · USA Nationwide

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FDA recallMedicationsClass II· SHANTOU Qiwei industrial Co., Ltd

MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++, Net content, 9g/0.32 oz, Manufactured by: Shantzu Qiwei Industry Co. Ltd, Add: Quiwei Building, Yingloinguan, Xiashan, Chaonan district, Shantou City, Guangdong Province, China Reason: cGMP Deviations Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · CA only

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Official feedMedications· FDA MedWatch safety alerts

Angiographic Catheter RecallThe maker or a government agency pulled this product. Check the model or lot number and stop using it until it's fixed or refunded.: Boston Scientific Removes Imager II Angiographic Catheters Boston Scientific Imager II Angiographic Catheters removed due to a manufacturing issue leading to tip detachment; could result in procedural delays, embolism

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