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Safety Reports: Blood

Updated:

Real Time Reports

Outbreak

Increase of Vibrio vulnificus infections in Florida following Hurricane Ian, Florida, USA

3 years ago •source lee.floridahealth.gov • details

Department of Health in Lee County (DOH-Lee) is urging the public to take precautions against infection and illness caused by Vibrio vulnificus following Hurricane Ian.

According to the DOH-Lee warning, Vibrio vulnificus is a bacterium that usually lives in warm, brackish sea water. These bacteria typically grow… See more

#blood #undercooked #raw #florida #unitedstates #fish #juice #seafood #oysters #cooks #specialk

Outbreak Increase of Vibrio vulnificus infections in Florida after Hurricane Ian Department of Health in Lee... photo #1
304   Comments Comment

Recall notice

Golden State Medical Supply Clopidogrel & Atenolol - recalled due to label mix-up, USA

3 years ago •source fda.gov • details

Golden State Medical Supply, Incorporated (GSMS, Inc.) - Camarillo, CA has initiated a voluntary recall of the products listed in the table below because a report was received that a bottle containing Clopidogrel 75mg Tablets produced with lot# GS046745 was mislabeled as Atenolol 25mg Tablets. This voluntary… See more

#blood #recall #drugs #unitedstates

Recalls Golden State Medical Supply Clopidogrel & Atenolol - recalled due to label mix-up Golden State Medic... photo #1
312   Comments Comment

Recall notice

My Stellar Lifestyle Wonder Pill Capsules - recalled due to undeclared tadalafil, USA

3 years ago •source fda.gov • details

Proper Trade LLC/My Stellar Lifestyle is voluntarily recalling Wonder Pill lot 20210912 and lot 31853-501, expiry 09/24, packaged in 10-count blisters co-packaged in a carton and in 60-count bottles to the consumer level. Proper Trade LLC/My Stellar Lifestyle was notified by Amazon that laboratory analysis has found… See more

#blood #recall #drugs #unitedstates #sub #ro-tel

Recalls My Stellar Lifestyle Wonder Pill Capsules - recalled due to undeclared tadalafil Proper Trade LLC/My... photo #1
312   Comments Comment
V

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

3 years ago •reported by user-vthc5199 • 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 #blood #dogfood #petfood #huntsville #alabama #unitedstates

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

Recall notice

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

3 years ago •source fda.gov • details

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

Recalls Antica Farmacista Ocean Citron Hand Sanitizer - recalled due to product contains benzene Salon Techn... photo #1
473   Comments Comment

Recall notice

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

3 years ago •source fda.gov • details

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

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

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

Recall notice

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

3 years ago •source fda.gov • details

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

#blood #pfizer #drugs #unitedstates #pita

Recalls Propofol Injection Emulsion, USP - recalled due to the presence of particulates Hospira, Inc., a Pfi... photo #1
312   Comments Comment

Recall notice

SANGTER Energy Supplement - recalled due to Undeclared Sildenafil, USA

3 years ago •source fda.gov • details

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

#blood #recall #drugs #unitedstates #sub

Recalls SANGTER Energy Supplement - recalled due to Undeclared Sildenafil DISTRIBUTOR RFR, LLC. is voluntari... photo #1
312   Comments Comment

Recall notice

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

3 years ago •source fda.gov • details

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

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

Recalls Banana Boat Sunscreen Spray - recalled due to due to presence of benzene Edgewell Personal Care Comp... photo #1
313   Comments Comment

Recall notice

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

3 years ago •source fda.gov • details

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

#blood #recall #drugs #unitedstates #sub

Recalls Dietary Supplement for Male Enhancement - recalled due to undeclared tadalafil Ultra Supplement LLC... photo #1
312   Comments Comment

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