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Safety Reports: Recall

Updated:

Nature’s Wonderland Thyroid Formula - recalled due to Salmonella, USA

3 days ago •source fda.gov • details

Recall notice

Penn Herb Company Ltd is recalling Nature’s Wonderland Thyroid Formula because it has the potential to be contaminated with Salmonella. The product was distributed through the Penn Herb Company Ltd website and retail store.

The recalled product is Nature’s Wonderland Thyroid Formula 51 bottles (60 Capsules per… See more

#recall #dietarysupplements #us #salmonella

Nature’s Wonderland Thyroid Formula - recalled due to Salmonella photo #1
320

Suntegrity Sunscreen foundation - recalled due to higher than acceptable microbiological mold count, USA

3 days ago •source fda.gov • details

Recall notice

On May 24, 2024, Suntegrity Skincare initiated a voluntary recall of nine lots of Suntegrity Impeccable Skin Sunscreen Foundation (Multiple Shades) based on its discovery of a higher-than-acceptable microbiological mold count (Species: Aspergillus Sydowii). The product was distributed online by the company and nationwide via retail stores.… See more

#recall #drugs #us

Suntegrity Sunscreen foundation - recalled due to higher than acceptable microbiological mold count photo #1
320

Ram It, To The Moon Dietary Supplements - recalled due to sildenafil and tadalafil, USA

4 days ago •source fda.gov • details

Recall notice

Integrity Products is voluntarily recalling the Ram It & To The Moon capsules to the consumer level. FDA analysis found these products to be tainted with sildenafil and Tadalafil. Ram It & To The Moon were distributed to consumers nationwide via the Internet.

Men with diabetes, high… See more

#dietarysupplements #recall #us

Ram It, To The Moon Dietary Supplements - recalled due to sildenafil and tadalafil photo #1
321

Multiple Brand Animal Feed Products - recalled due to elevated levels of several chemicels, USA

4 days ago •source fda.gov • details

Recall notice

ADM Animal Nutrition, a division of ADM (NYSE: ADM), is expanding the recalls announced on March, 30, 2024 and April 11, 2024, to include the following additional products due to elevated levels of magnesium, sodium, calcium, chloride and/or phosphorus from several brands, Grostrong, MoorMan's, MaxLean, Roughage Buster,… See more

#recall #petfood #us

Multiple Brand Animal Feed Products - recalled due to elevated levels of several chemicels photo #1
321

StellaLife Inc. Homeopathic StellaLife Oral Care Products - recalled due to microbial contamination, USA

1 week ago •source fda.gov • details

Recall notice

HomeoCare Laboratories Inc. is voluntarily recalling two batches of Homeopathic StellaLife Oral Care Products manufactured in 2024 due to FDA findings of microbial contamination. This recall is to be performed at the consumer level. The affected products were manufactured at HomeoCare Laboratories, shipped nationwide to our customers,… See more

#recall #drugs #us

StellaLife Inc. Homeopathic StellaLife Oral Care Products - recalled due to microbial contamination photo #1
321

Medline SubG Endotracheal Tubes with Subglottic Suction - recalled due to potential malfunction, USA

2 weeks ago •source fda.gov • details

Recall notice

Medline Industries, LP initiated a nationwide recall of 6 SubG Endotracheal Tubes with Subglottic Suction and 10 kits that contain these devices. The inflation tube and other device components have become detached and/or torn from the main tube, resulting in moisture buildup, loss of pressure, or inability… See more

#medicaldevices #recall #us

Medline SubG Endotracheal Tubes with Subglottic Suction - recalled due to potential malfunction photo #1
321

Sagent Docetaxel Injection, USP - recalled due to presence of particulate matter, USA

2 weeks ago •source fda.gov • details

Recall notice

Sagent Pharmaceuticals today announced the voluntary recall of two lots of Docetaxel Injection, USP to the User Level as the result of a customer complaint due to the potential presence of particulate matter from the stopper in the drug product. The product was distributed by Sagent Pharmaceuticals… See more

#recall #drugs #us

Sagent Docetaxel Injection, USP - recalled due to presence of particulate matter photo #1
322

NÜTRL Tumbler Cup recalled due to potential chemical and ingestion hazards, Canada

2 weeks ago •source recalls-rappels.canada.ca • details

Recall notice

NÜTRL, a popular beverage brand, has issued a recall for its 30 oz. stainless steel tumbler cups due to potential chemical and ingestion hazards. The recall was initiated after several consumers reported illnesses linked to the product. As of May 23, 2024, Sunscope has received 43 reports… See more

#recall #ca

NÜTRL Tumbler Cup recalled due to potential chemical and ingestion hazards photo #1
86

Hospira Buprenorphine Hydrochloride Injection and Labetalol Hydrochloride Injection - recalled due to Packaging Defect, USA

3 weeks ago •source fda.gov • details

Recall notice

Hospira, Inc., a Pfizer company (“Pfizer”), is voluntarily recalling the lots listed in the table below of Buprenorphine Hydrochloride Injection CarpujectTM Units and Labetalol Hydrochloride Injection, USP CarpujectTM Units to the User level. The recall was initiated due to the potential for incomplete crimp seals; one customer… See more

#pfizer #recall #drugs #us

Hospira Buprenorphine Hydrochloride Injection and Labetalol Hydrochloride Injection - recalled due to Packaging Defect photo #1
321

Ethicon Megadyne Mega Soft Pediatric Patient Return Electrode - recalled due to Reports of patient burn injuries, USA

1 month ago •source fda.gov • details

Recall notice

MEGADYNE™ is initiating a voluntary recall of all MEGADYNE™ MEGA SOFT™ Pediatric Patient Return Electrodes. The product is being removed because Megadyne has received reports of patient burn injuries in procedures where the Mega Soft Patient Return Electrodes were used. A root cause investigation on the reports… See more

#recall #medicaldevices #us

Ethicon Megadyne Mega Soft Pediatric Patient Return Electrode - recalled due to Reports of patient burn injuries photo #1
321

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