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Blood

Updated:

Lupin Quinapril tablets - recalled due to nitrosamine impurity, USA

1 year ago •source fda.gov • details

Recall notice

Lupin Pharmaceuticals Inc. is voluntarily recalling four (4) lots of Quinapril Tablets to the patient (consumer/user) level due to the presence of a nitrosamine impurity, N-Nitroso-Quinapril, observed in recent testing above the Acceptable Daily Intake (ADI) level. To date, Lupin has received no reports of illness that… See more

#blood #drugs #us #vegetable #meat #ro-tel

Lupin Quinapril tablets - recalled due to nitrosamine impurity photo #1
322
C

Dreambone wrapped in chicken, Fredericktown, MO, USA

1 year ago •reported by user-cbbyk266 • details

I had every pet parents worst nightmare and almost lost my daughter I birthed from my Pomeranian. I have had her 6 years and normally don't change her diet or treats but mom's friend give princess a dreambone and princess loved it so I started buying them… See more

#blood #fredericktown #missouri #us #er #lays #ro-tel

Dreambone wrapped in chicken photo #1
4

ByHeart Whole Nutrition Infant Formula - recalled due to Cronobacter Akasaki, USA

1 year ago •source fda.gov • details

Recall notice

The product being recalled is ByHeart Whole Nutrition Infant Formula, Milk Based Powder with Iron for 0-12 Months in 24 oz containers. The formula under voluntary recall was distributed directly to consumers in the U.S. and can be identified by the number on the bottom of the… See more

#blood #recall #us #milk #actii

ByHeart Whole Nutrition Infant Formula - recalled due to Cronobacter Akasaki photo #1
322
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DreamBone treats almost killed all 3 of my dogs!, La Vernia, Texas, USA

1 year ago •reported by user-nnxt4114 • details

We bought these treats for our dogs as rewards and they all started getting sick. Started with vomiting and diarrhea. My labs are tougher and started to get better but my Doberman almost died. I had to take him to the vet twice, the first time on… See more

#dreambonedogtreats #blood #dogfood #petfood #lavernia #texas #us

92
H

DreamBone spirals that maybe contaminated in some way, Queen Creek, AZ, USA

1 year ago •reported by user-hvghh941 • details

Both of my female Dachshunds were fed one spiral each in the late morning on a Tuesday. These came from a bag just opened at this time. Their night feeding was OK and there was NO change in their food or water. On Wednesday morning neither dog… See more

#blood #queencreek #arizona #us #buffalo #chicken #bowl #ro-tel #cooks #bluebuffalo

389

Mylan Institutional LLC Octreotide Acetate Injection - recalled due to due to glass particulates, USA

1 year ago •source fda.gov • details

Recall notice

Mylan Institutional LLC, a Viatris company, is voluntarily recalling lot AJ21002, exp 3/2024, of Octreotide Acetate Injection, 500 mcg/mL, packaged in a carton of ten 1mL syringes. This lot is being recalled at the user (hospital/pharmacy) level due to a product complaint of the presence of glass… See more

#blood #drugs #us #pita #sub

322

Aurobindo Pharma Quinapril and Hydrochlorothiazide Tablets - recalled due to due to presence of impurities, USA

1 year ago •source fda.gov • details

Recall notice

East Windsor, New Jersey, Aurobindo Pharma USA, Inc. has initiated a voluntary recall of two (2) lots (refer table below) of Quinapril and Hydrochlorothiazide Tablets USP 20mg / 12.5mg, to the consumer level from the US market due to presence of Nitrosamine Drug Substance Related Impurity (NDSRI),… See more

#blood #drugs #us #sub #vegetable #meat #ro-tel

Aurobindo Pharma Quinapril and Hydrochlorothiazide Tablets - recalled due to due to presence of impurities photo #1
322

WatchCare Incontinence management system - Urgent Medical Device Correction due to potential RF interference with other medical devices, 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 WatchCare Incontinence Management System due to potential for radio frequency (RF) interference with other medical devices. The WatchCare System is distributed in the United States.

This Urgent Medical Device Correction applies to… See more

#blood #medicaldevices #us #feta #lays #ro-tel

WatchCare Incontinence management system - Urgent Medical Device Correction due to potential RF interference with other medical devices photo #1
322

Unilever Dry Shampoo Aerosol - recalled due to Product Safety/Unapproved Ingredient, USA

1 year ago •source fda.gov • details

Recall notice

Unilever United States today issued a voluntary product recall to the consumer level of select lot codes of dry shampoo aerosol products produced prior to October 2021 from Dove, Nexxus, Suave, TIGI (Rockaholic and Bed Head), and TRESemmé due to potentially elevated levels of benzene. The recalled… See more

#blood #us #ham

Unilever Dry Shampoo Aerosol - recalled due to Product Safety/Unapproved Ingredient photo #1
324

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