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Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

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

1 year ago •source fda.gov • details

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 #unitedstates

Recalls Ethicon Megadyne Mega Soft Pediatric Patient Return Electrode - recalled due to Reports of patient b... photo #1
312   Comments Comment

Recall notice

Dr. Reddy's Sapropterin Dihydrochloride Powder for Oral Solution - recalled due to decreased potency, USA

1 year ago •source fda.gov • details

Dr. Reddy's Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY, NSEIFSC: DRREDDY, along with its subsidiaries together referred to as "Dr. Reddy's"), today announced that it is voluntarily recalling six (6) lots of Sapropterin Dihydrochloride Powder for Oral Solution 100 mg to the consumer level due to… See more

#ketogummiesscam #scam #blood #recall #drugs #unitedstates

Recalls Dr. Reddy’s Sapropterin Dihydrochloride Powder for Oral Solution - recalled due to decreased potency... photo #1
312   Comments Comment

Recall notice

Schwinnng Herbal Dietary Supplement - recalled due to contamination with Nortadalafil, USA

1 year ago •source fda.gov • details

STOP CLOPEZ CORP is voluntarily recalling one lot of Schwinnng capsules to the consumer level. FDA analysis has found the Schwinnng products to contain Nortadalafil. Nortadalafil is an active drug ingredient known for the treatment of male erectile dysfunction. The presence of Nortadalafil in Schwinnng capsules makes… See more

#recall #drugs #unitedstates

Recalls Schwinnng Herbal Dietary Supplement - recalled due to contamination with Nortadalafil STOP CLOPEZ CO... photo #1
312   Comments Comment

Recall notice

Nutrena Country Feeds Meat bird 22% Crumble (RV) - recalled due to non-inclusion of vitamin D, Bryson City, North Carolina, USA

1 year ago •source fda.gov • details

Cargill’s animal nutrition business is conducting a voluntary recall of Nutrena® Country Feeds® Meat bird 22% Crumble (RV) due to non-inclusion of Vitamin D. The affected products were manufactured and sold in the eastern United States and are being recalled from retail outlets in the Alabama, Georgia,… See more

#recall #petfood #cargill #brysoncity #northcarolina #unitedstates

Recalls Nutrena Country Feeds Meat bird 22% Crumble (RV) - recalled due to non-inclusion of vitamin D Cargil... photo #1
1   Comments Comment

Recall notice

ADM Animal Nutrition Chicken, Swine and Rabbit Feed Products Update - recalled due elevated levels of minerals, USA

1 year ago •source fda.gov • details

ADM Animal Nutrition, a division of ADM (NYSE: ADM), is expanding the recall announced on March, 30, 2024, to include the following additional products due to elevated levels of magnesium, sodium, calcium and/or phosphorus: Pen Pals® Chicken Starter-Grower (Product Nos.70009AAA46 and 70009AAA44); Pen Pals Egg Maker Complete… See more

#recall #petfood #unitedstates

Recalls ADM Animal Nutrition Chicken, Swine and Rabbit Feed Products Update - recalled due elevated levels o... photo #1
  Comments Comment

Recall notice

Tejocote Dietary Supplements - recalled because it contains toxic yellow oleander, USA

1 year ago •source fda.gov • details

Global Mix, Inc. of New York, is recalling tejocote products to include the following brands: Eva Nutrition, Science of Alpha, Niwali, NWL Nutra. The recalled products are labeled as tejocote root but are toxic yellow oleander. The recalled products were distributed in the following states: AL, AK,… See more

#recall #unitedstates

Recalls Tejocote Dietary Supplements - recalled because it contains toxic yellow oleander Global Mix, Inc. o... photo #1
312   Comments Comment

Recall notice

Medline and Centurion Convenience kits - recalled due to lack of sterility, USA

1 year ago •source fda.gov • details

In direct response to the Nurse Assist, LLC voluntary product recall initiated on November 6, 2023, for saline and sterile water medical products, Medline Industries, LP initiated a nationwide recall on November 15, 2023, for its Medline and Centurion branded convenience kits containing Nurse Assist 0.9% Sodium… See more

#recall #medicaldevices #unitedstates

Recalls Medline and Centurion Convenience kits - recalled due to lack of sterility In direct response to the... photo #1
312   Comments Comment

Recall notice

Tide, Gain, Ace, and Ariel Detergent Packets recalled due to Risk of Serious Injury, USA

1 year ago •source cpsc.gov • details

Procter & Gamble has issued a recall for 8.2 million bags of Tide, Gain, Ace, and Ariel laundry detergent pods due to a risk of serious injury. The packaging of these products can split open, posing a risk if the contents are ingested or come into contact… See more

#recall #unitedstates

Recalls Tide, Gain, Ace, and Ariel Detergent Packets recalled due to Risk of Serious Injury Procter & Gamble... photo #1
312   Comments Comment

Recall notice

Aruba Aloe Hand Sanitizer Gel and Alcoholada Gel - recalled because they contain Methanol, USA

1 year ago •source fda.gov • details

Aruba Aloe Balm N.V. is voluntarily recalling 40 lots of Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel to the consumer level. The products have been found to contain alcohol denatured with methanol. Products were distributed between 5/1/2021 and 10/27/2023 and sold in… See more

#recall #unitedstates

Recalls Aruba Aloe Hand Sanitizer Gel and Alcoholada Gel - recalled because they contain Methanol Aruba Aloe... photo #1
312   Comments Comment

Recall notice

Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance, USA

1 year ago •source fda.gov • details

Honeywell Safety Products USA, Inc. is voluntarily recalling Fendall 2000 Non-Sterile Eyewash Cartridge for the Fendall 2000 Eyewash Station. This recall is being conducted at the industrial consumer level. Honeywell’s supplier of the Fendall 2000 Non-Sterile Eyewash Cartridge has been found to be non-compliant with current good… See more

#recall #drugs #unitedstates

Recalls Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance Honeywell Safety Products U... photo #1
312   Comments Comment

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