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Safety Reports: Blood

Updated:

Recent Reports

Ascend Laboratories Dabigatran Etexilate Capsules - recalled due to Detection of N-Nitrosodimethylamine Impurity, USA

1 year ago •source fda.gov • details

Recall notice

Ascend Laboratories LLC. is voluntarily recalling Dabigatran Etcxilate Capsules. USP 75 mg and 150 mg to the consumer/user level due to the presence of a nitrosamine. N-nitroso-dabigatran, above the established Acceptable Daily Intake (ADI) level. The product lots were distributed nationwide to wholesalers, Distributors and Retailers (dispensers)… See more

#blood #drugs #unitedstates

Ascend Laboratories Dabigatran Etexilate Capsules - recalled due to Detection of N-Nitrosodimethylamine Impurity photo #1
312
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The complete unsanitary of Modern Meats in Humboldt Sask, Modern Meat & Abattoir (78) LTD, Main St, Humboldt, SK, Canada

1 year ago •reported by user-wkkz6344 • details

I was working there and only last a couple weeks. The filth. I’ve never seen a place of business especially one where food is being handled. In the far back cooler the is raw meet over cooked meat. The amount of rotting blood on the floor was so gross. And owner does not care

#foodsafetyissue #raw #blood #cleanliness #510mainstreet #humboldt #saskatchewan #canada

2

Life2000 Ventilation System - recalled due to patient oxygen desaturation, USA

1 year ago •source fda.gov • details

Recall notice

Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for the Life2000 Ventilation System due to the potential for patient oxygen desaturation (low blood oxygen) events that can occur under certain conditions when the Life2000 system is connected with a third-party oxygen concentrator.… See more

#blood #recall #medicaldevices #unitedstates #pita

312
H

PRO Apixiban by Pro Doc, South Shore, QC, Canada

1 year ago •reported by user-hhkgt152 • details

Was given a generic to Eliquis blood thinner called PRO Apixiban. The government will no longer cover Eliquis and it’s a life essential medication. But, sending billions overseas makes more sense.
One dose made me very ill for 22 days. It started with heart burn, gas, then… See more

#blood #medicaldevices #quebeccity #quebec #canada #sub #ro-tel

77

Bindle Bottle LLC Bottles - recalled due to Adulterated by lead, USA

1 year ago •source fda.gov • details

Recall notice

Bindle Bottle LLC of Carlsbad, CA, is recalling its Bindle Bottles because they may contain an area of exposed lead located in the bottom storage compartment of the bottle. Unpackaged food stored in the bottom storage compartment of the bottle may have been adulterated by the lead… See more

#blood #recall #unitedstates #sub #chi-chis

Bindle Bottle LLC Bottles - recalled due to Adulterated by lead photo #1
312

PrimeZEN Black 6000 male enhancement capsules - recalled due to undeclared ingredients, USA

1 year ago •source fda.gov • details

Recall notice

Volt Candy is voluntarily recalling one lot of PrimeZen Black 6000, 2000 mg capsule, to the consumer level. FDA analysis has found PrimeZen Black 6000 capsules to be tainted with sildenafil & tadalafil. Sildenafil and tadalafil are phosphodiesterase (PDE-5) inhibitors found in FDA-approved products for the treatment… See more

#blood #recall #drugs #unitedstates #sub

PrimeZEN Black 6000 male enhancement capsules - recalled due to undeclared ingredients photo #1
312

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