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Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

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

1 year ago •source fda.gov • details

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

#recall #medicaldevices #unitedstates

Recalls Medline SubG Endotracheal Tubes with Subglottic Suction - recalled due to potential malfunction Medl... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

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 #unitedstates

Recalls Sagent Docetaxel Injection, USP - recalled due to presence of particulate matter Sagent Pharmaceutic... photo #1
313   Comments Comment

Recall notice

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

1 year ago •source recalls-rappels.canada.ca • details

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 #canada

Recalls NÜTRL Tumbler Cup recalled due to potential chemical and ingestion hazards NÜTRL, a popular beverage... photo #1
87   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

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 #unitedstates

Recalls Hospira Buprenorphine Hydrochloride Injection and Labetalol Hydrochloride Injection - recalled due t... photo #1
312   Comments Comment

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

#petfood #cargill #recall #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

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