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Safety Reports: Blood

Updated:

Real Time Reports

A

My Yorkie is in the hospital fighting for her life after eating Dream bones. She's bleeding from the rectum severely., Huntsville, Alabama, USA

2 years ago • details

She began to have diarrhea 3 days ago after eating the first Dream bone. We didn't relate the problem. She got a second one the next day and the diarrhea continued for 3 days. Last night blood began to pour from her. Today they are trying to see where the bleeding is coming from to save her.  | Symptoms: Diarrhea, Bloody Stool

#dreambonedogtreats #petfood #dogfood #blood #huntsville #alabama #unitedstates

My Yorkie is in the hospital fighting for her life after eating Dream bones. She's bleeding from the rectum severely. photo #1
  Comments Comment

Antica Farmacista Ocean Citron Hand Sanitizer - recalled due to product contains benzene, Seattle, WA, USA

2 years ago •source fda.gov • details

Recall notice

Salon Technologies International. Inc. is voluntarily recalling one lot of Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%, Lot 1166A. Expiration 6/18/2023 to the consumer level. Firm lab testing has found the product to contain benzene. Benzene is classified as a human carcinogen. Exposure to benzene can… See more

#drugs #blood #seattle #washington #unitedstates

Antica Farmacista Ocean Citron Hand Sanitizer - recalled due to product contains benzene photo #1
1   Comments Comment

Philips Respironics CPAP or Bi-Level PAP therapy masks - recalled due to potential risk of serious injury, USA

2 years ago •source fda.gov • details

Recall notice

These masks may continue to be used according to the updated instructions and labeling if patients or people in close proximity to them do not have implanted metallic medical devices or metallic objects in the body.

Royal Philips’ (NYSE: PHG; AEX: PHIA) subsidiary Philips Respironics is alerting… See more

#medicaldevices #recall #blood #unitedstates #sub #hunts

Philips Respironics CPAP or Bi-Level PAP therapy masks - recalled due to potential risk of serious injury photo #1
  Comments Comment

Propofol Injection Emulsion, USP - recalled due to the presence of particulates, USA

2 years ago •source fda.gov • details

Recall notice

Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Propofol Injectable Emulsion (containing benzyl alcohol), 100mL Single Patient Use Glass Fliptop Vial; lot EA7470, to the user level due to visible particulates observed in two vials during annual examination of retention samples. The product lot… See more

#drugs #pfizer #blood #unitedstates #pita

Propofol Injection Emulsion, USP - recalled due to the presence of particulates photo #1
  Comments Comment

SANGTER Energy Supplement - recalled due to Undeclared Sildenafil, USA

2 years ago •source fda.gov • details

Recall notice

DISTRIBUTOR RFR, LLC. is voluntarily recalling lot #48656, Exp. 01/2025 of SANGTER Energy Supplement, 3000 mg, packaged in 7-count blister packs within a carton to the consumer level. FDA analysis has found the product to contain undeclared sildenafil. Sildenafil is a phosphodiesterase (PDE-5) inhibitor found in FDA-approved… See more

#drugs #recall #blood #unitedstates #sub

SANGTER Energy Supplement - recalled due to Undeclared Sildenafil photo #1
  Comments Comment

Banana Boat Sunscreen Spray - recalled due to due to presence of benzene, USA

2 years ago •source fda.gov • details

Recall notice

Edgewell Personal Care Company (NYSE: EPC) today issued a voluntary nationwide recall of three batches of Banana Boat Hair & Scalp Sunscreen Spray SPF 30 to the consumer level as outlined in the list below. An internal review found that some samples of the product contained trace… See more

#recall #blood #unitedstates #banana #ro-tel

Banana Boat Sunscreen Spray - recalled due to due to presence of benzene photo #1
1   Comments Comment

Dietary Supplement for Male Enhancement - recalled due to undeclared tadalafil, USA

2 years ago •source fda.gov • details

Recall notice

Ultra Supplement LLC is voluntarily recalling lot number DAP272109, exp 4/1/26 of Sustango capsules packaged in 10-count blisters packaged in a carton to the consumer level. Ultra Supplement was notified by Amazon that laboratory analysis has found the product to be tainted with tadalafil, an ingredient in… See more

#drugs #recall #blood #unitedstates #sub

Dietary Supplement for Male Enhancement - recalled due to undeclared tadalafil photo #1
  Comments Comment

MKS Enterprise LLC Honey - recalled due to undeclared active pharmaceutical ingredient tadalafil, USA

2 years ago •source fda.gov • details

Recall notice

This product was found to contain the undeclared active pharmaceutical ingredient tadalafil. Tadalafil, which is a phosphodiesterase type-5 (PDE-5) inhibitor, is the active ingredient in an FDA-approved prescription drug, used to treat erectile dysfunction (ED). Product was sold through our website, wholesaleonline1.com Mar 2022 to July 2022… See more

#recall #blood #unitedstates #honey

MKS Enterprise LLC Honey - recalled due to undeclared active pharmaceutical ingredient tadalafil photo #1
  Comments Comment

Kingdom Honey Royal Honey VIP - recalled due to Undeclared Sildenafil, USA

2 years ago •source fda.gov • details

Recall notice

Shopaax.com in Newark, DE is voluntarily recalling all lots of Kingdom Honey Royal Honey VIP because it contains undeclared Sildenafil, the active ingredient in the FDA-approved prescription drug Viagra, used to treat erectile dysfunction. FDA approval of Viagra is restricted to use under the supervision of a… See more

#recall #blood #unitedstates #honey #ro-tel

Kingdom Honey Royal Honey VIP - recalled due to Undeclared Sildenafil photo #1
  Comments Comment

Pfizer Propofol Injection Emulsion, USP - recalled due to Potential presence of visible particulate, USA

2 years ago •source fda.gov • details

Recall notice

Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Propofol Injectable Emulsion, USP (containing benzyl alcohol), 100 mL Single Patient Use Glass Fliptop Vial; lot DX9067, to the user level due to a visible particulate observed in a single vial during annual examination of retain… See more

#drugs #recall #pfizer #blood #unitedstates #pita

Pfizer Propofol Injection Emulsion, USP - recalled due to Potential presence of visible particulate photo #1
  Comments Comment

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