foundmatterdb

Field reports on stuff that let you down

Medications

394 reports

YouTubeMedications

Stick Detective S1E05: The Wrong Pills | English B2 Mystery A bottle. A label. And pills that were not his. Listen to the story first, then learn the vocabulary and the grammar from it. English ...

flagged: wrong pills
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YouTubeMedications

Typhoid ke baare me...#typhoidvaccine #typhoidsymptoms #fever #disease # #pharmacy #bpharma Typhoid Fever | Causes, Symptoms & Prevention Typhoid fever is a bacterial infection caused by Salmonella Typhi. It commonly ...

flagged: bacterial
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BlueskyMedications

Monstober 2026 Day 22 - Napole and Napfibian! Their river habitat was unfortunately contaminated by a pharmaceutical company dumping sleeping pills. They live in a constant state of sleepfloating by producing oversized bubbles through their nostrils. #monstober #pixelart

flagged: contaminated
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FDA drug shortageMedications· Epic Pharma, LLC

Shortage: Rifampin Capsule — Rifampin, Capsule, 300 mg (NDC 42806-799-30) Status: Current Reason: Discontinuation of the manufacture of the drug Used for: Anti-Infective

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FDA drug shortageMedications· Teva Pharmaceuticals USA, Inc.

Shortage: Clonazepam Tablet — Clonazepam, Tablet, .5 mg (NDC 0093-0832-05) Status: Current Used for: Neurology, Pediatric, Psychiatry

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YouTubeMedicationstylenolAlternatives →tylenol

7 People Took Tylenol3 reports about tylenol on this site. See them all →. All 7 Died. (1982) In September 1982, seven Chicago-area residents died after taking cyanide-contaminated Tylenol capsules. Police issued urgent ...

flagged: contaminated
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BlueskyMedicationseye dropAlternatives →high

Ophthopedia Update: Contaminated, counterfeit eye drops18 reports about eye drop on this site. See them all → being sold in US, FDAU.S. Food and Drug Administration. It handles food, drink, cosmetic and medication recalls. Learn more → warns: Editor’s note: This is a developing news story. Please check back soon for updates. Several counterfeit eye drops, some of which were contaminated with bacteria, were recently found in U.S. stores, according to a…

flagged: contaminated, bacteria, fda
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BlueskyMedicationseye dropAlternatives →high

Ophthopedia Update: Contaminated, counterfeit eye drops18 reports about eye drop on this site. See them all → being sold in US, FDAU.S. Food and Drug Administration. It handles food, drink, cosmetic and medication recalls. Learn more → warns: Editor’s note: This is a developing news story. Please check back soon for updates. Several counterfeit eye drops, some of which were contaminated with bacteria, were recently found in… #ophthalmology #eye #eyenews

flagged: contaminated, bacteria, fda
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YouTubeMedicationstylenolAlternatives →tylenol

7 People Killed by POISONED Tylenol3 reports about tylenol on this site. See them all → — Killer Never Found In 1982, seven people died in the Chicago area after taking Tylenol capsules contaminated with cyanide. The murders triggered a ...

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Is Your Fiber Supplement Contaminated? ⚠️ Your daily fiber supplement might contain heavy metals. ⚠️ Tim Ferriss breaks down contamination in common psyllium husk ...

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BlueskyMedications

DIY healthcare is on the rise – here’s why it’s so dangerous theconversation.com/diy-healthca... So many harms, including: 👉 "...delayed access to professional support." 👉 marketing of unproven products / advice 👉 contaminated, "counterfeit & substandard medicines" 👉 marketing of distrust

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FDA device recallMedications· Howmedica Osteonics Corp.

TS Universal Baseplate Finishing Tray, Triathlon. Catalog Number: 6543-6-506. Reason: Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual moisture remaining after sterilization. Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongo…

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FDA device recallMedications· Ferno-Washington Inc

Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816 and PowerX2 Premium, Item No. 0015821 Reason: Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system not operating in powered mode, or …

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FDA device recallMedications· Howmedica Osteonics Corp.

Triathlon Hinge Femoral Prep Tray. Catalog Number: 6543-6-514. Reason: Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual moisture remaining after sterilization. Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · These tra…

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FDA device recallMedications· Medline Industries, LP

Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A & B, Medline Product number/SKU DYNJ04584L; 2) OPEN HEART ACCESSORY PACK, Medline Product number/SKU DYNJT5715A; 3) CABG ACCESSORY PACK, Medline Product number/SKU DYNJ85751; 4) OPEN HEART PACK, Medline Product number/SKU DYNJ53741N; 5) OPEN HEART PACK 1&2, Medline Product number/SKU…

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FDA device recallMedications· Instrumentation Laboratory

HemoslL AcuStar HIT-lgG(PF-4). Part Number: 0009802028. in vitro diagnostic (OUS only) Reason: Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples. Class IThe FDA's most serious recall level: a reasonable chance the product could cause serious health problems or death. · Ongoing · Worldwide - US Nationwide distribution in the states of AR, AZ, CA, CT, FL, GA, MA, MD, NJ, NY, PA, RI, TN, WA, WV and the countries of Austria, Be…

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FDA device recallMedications· Cook Incorporated

Williams Cystoscopic Injection Needles, used for cystoscopic injection into the urethra, bladder neck, and bladder wall, Reference Part Number 090001-S26, Order Number (GPN) G16112 Reason: The female Luer lock adapter component in the affected device lots may not have been correctly seated due to misalignment and inadequate torquing during manufacturing. Po…

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FDA device recallMedications· Medtronic Sofamor Danek USA Inc

Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with an inert additive to yield a demineralized bone matrix (DBM) allograft product having a particular physical form and/or handling property. Grafton DBM Gel and Grafton Plus DBM Paste are produced from a powder form of DBM, while Grafton DBM Flex, Putty, Matrix, Crunch" a…

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FDA device recallMedications· Medline Industries, LP

Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A Reason: Discrepancy in the shelf-life of a component Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · US Nationwide distribution in the state of NY.

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FDA device recallMedications· Medline Industries, LP

Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A CHN GYN ONCOLOGY DYNJ906731M Reason: Kits contain CONMED AirSeal Access Ports. The ports were recalledThe maker or a government agency pulled this product. Check the model or lot number and stop using it until it's fixed or refunded. by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures. Class IThe FDA's most serious recall level: a reasonable chance the product could cause serious health problems or death.…

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FDA device recallMedications· Medline Industries, LP

Medline surgical convenience kits labeled as: OPEN HEART, Medline Product Number/SKU DYNJ902898D Reason: Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use. Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · US Nationwide distribution.

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FDA device recallMedications· Medline Industries, LP

Medline surgical convenience kits labeled as: VEIN HARVESTING PACK, Medline product number/SKU DYNJ51845D Reason: Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use. Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · US Nationwide distribution.

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FDA device recallMedications· Magellan Diagnostics, Inc.

LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762. Reason: In kit sub-lot 2530M-01 the date of expiration printed on the outer labeling may indicate the wrong expiration date of July 22, 2026 while the correct expiration date is July 13, 2026. If used the system will display an error message and prevent the operator from running the test. Resu…

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FDA device recallMedications· Baxter Healthcare Corporation

Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product Description: LIKORALL 242 ES, NATURAL Product Code: 3122005NA Product Description: LIKORALL 242 ES, NATURAL Product Code: 3122006 Product Description: LIKORALL 242 ES, WHITE Product Code: 3122006NA Product Description: LIKORALL…

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FDA device recallMedications· Beckman Coulter, Inc.

DxU 840m Iris, REF: C76947; DxU 850m Iris, REF: C49513 Reason: The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however, the check valve replacement was excluded from the annual preventive maintenance (PM) requirements without adequate reliability evaluatio…

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FDA device recallMedications· Medline Industries, LP

Convenience Kits containing CONMED AirSeal Access Ports CHN GYN ONCOLOGY DYNJ906731K DYNJ906731L DYNJ906731N DAVINCI PROSTATECTOMY DYNJG901002A DYNJG901002B DYNJG901002C DYNJG901002D GENERAL DAVINCI DYNJG901004B DYNJG901004D HERNANDEZ DAVINCI ACC BUNDLE M DYNJ911258A KIT ROBOTICS UROLOGY PROSTATE …

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FDA device recallMedications· Medline Industries, LP

Medline surgical convenience kits labeled as: 1) NEURO-SPINE BASIN PACK, Medline Product Number/SKU DYNJ80055A; 2) AV SHUNT PACK-LF, Medline Product Number/SKU DYNJ24528M. Reason: Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking…

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FDA device recallMedications· Medline Industries, LP

Medline surgical convenience kits labeled as: 1) OPEN HEART CDS, Medline product number/SKU CDS840094R; 2) OPEN HEART CDS, Medline product number/SKU CDS840171AG; 3) MHC AV FISTULA, Medline product number/SKU DYNJ903705K; 4) PERIPHERAL VASC MAJR-LF, Medline product number/SKU CDS840379O; 5) MINOR VASCULAR PACK-LF, Medline product number/SKU DYNJ0…

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FDA device recallMedications· Medline Industries, LP

Medline surgical convenience kits labeled as: 1) MAIN/LAPAROSCOPY TRANSPLA PACK, Medline product number/SKU DYNJ0656274AC; 2) MAIN/LAPAROSCOPY TRANSPLA PACK, Medline product number/SKU DYNJ0656274AB; 3) CATH LAB ENDO AAA, Medline product number/SKU DYNJ35312I; 4) MAIN/LAPAROSCOPY TRANSPLA PACK, Medline product number/SKU DYNJ0656274AA. Reason: Medi…

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FDA device recallMedications· Medtronic Sofamor Danek USA Inc

Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with an inert additive to yield a demineralized bone matrix (DBM) allograft product having a particular physical form and/or handling property. Grafton DBM Gel and Grafton Plus DBM Paste are produced from a powder form of DBM, while Grafton DBM Flex, Putty, Matrix, Crunc…

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