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Safety Reports: Recall

Updated: November 9, 2021 4:04 PM

Real Time Reports

Recall notice

Dietary Supplement Protein Powder - recalled due to undeclared allergen, USA

4 years ago •source fda.gov • details

Nutracap Holdings, LLC of Norcross, Georgia is voluntarily recalling various dietary supplements due to undeclared wheat, milk, soy and/or coconut on the labels. People who have an allergy or severe sensitivity to soy, milk, wheat, or coconut run the risk of serious or life-threatening allergic reaction if… See more

#peanutallergy #milkallergy #wheatallergy #soyallergy #recall #unitedstates #chocolate #vegan #butter #milk #soy #sugar #peanutbutter

Recalls Dietary Supplement Protein Powder - recalled due to undeclared allergen Nutracap Holdings, LLC of No... photo #1

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Recall notice

MaryRuth’s liquid probiotic for infants - recalled due to Pseudomonas aeruginosa, USA

4 years ago •source fda.gov • details

MaryRuth’s, a leading omni-channel health and wellness brand that offers vitamins, minerals, and supplements for the entire family, today announced that, out of an abundance of caution, it is voluntarily recalling two lots of its liquid probiotic for infants (1oz) due to the possibility of contamination by… See more

#probiotics #recall #amazon #target #unitedstates

Recalls MaryRuth’s liquid probiotic for infants - recalled due to Pseudomonas aeruginosa MaryRuth’s, a leadi... photo #1

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Recall notice

Purina Animal Supplement feed - recalled due to potential of elevated urea levels, Texas, USA

4 years ago •source fda.gov • details

Purina Animal Nutrition is voluntarily recalling one lot of the following products for cattle livestock and for wildlife such as deer, antelope, and wild sheep due to the potential of elevated urea levels. The affected products include:

- Formula No. 376C . Description: Purina® PRECON Cattle Starter.… See more

#recall #texas #unitedstates

Recalls Purina Animal Supplement feed - recalled due to potential of elevated urea levels Purina Animal Nutr... photo #1

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Recall notice

Cardinal Health’s Monoject™ Prefilled Syringes - recalled due to potential air draw back, USA

4 years ago •source fda.gov • details

On August 19, 2021, Aligned Medical Solutions initiated a nationwide recall of Cardinal Health’s Monoject™ Flush Prefilled Saline Syringes placed into 9,378 kits. Including:
- 1 lot of AMS-9041CP Leaderflex Insertion Kit with Ultrasound
- 1 lot of AMS-9046CP-1 Insertion Tray-RX
- 45 lots of AMS8939A Universal… See more

#recall #medicaldevices #unitedstates

Recalls Cardinal Health’s Monoject™ Prefilled Syringes - recalled due to potential air draw back On August 1... photo #1

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Recall notice

artnaturals Scent Free Hand Sanitizer - recalled due to due to impurities, USA

4 years ago •source fda.gov • details

artnaturals is voluntarily recalling ten manufacturing lots of artnaturals 8oz Scent Free Hand Sanitizer. FDA testing identified 8oz bottles of Scent Free Hand Sanitizer from a single manufacturing lot: G20128A, contained several impurities. Upon being contacted by the FDA, artnaturals responded immediately to proactively address the matter… See more

#recall #blood #handsanitizer #unitedstates

Recalls artnaturals Scent Free Hand Sanitizer - recalled due to due to impurities artnaturals is voluntarily... photo #1

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Recall notice

Merck CUBICIN® 500mg - recalled due to Product contains glass, USA

4 years ago •source fda.gov • details

KENILWORTH, N.J., Oct. 19, 2021 – Merck (NYSE: MRK), known as MSD outside the United States and Canada, is voluntarily recalling one lot of CUBICIN® (daptomycin for injection) 500mg for intravenous use, Lot 934778, Exp June 2022. Because treatment with CUBICIN is likely to be initiated at… See more

#blood #recall #drugs #unitedstates #cake

Recalls Merck CUBICIN® 500mg - recalled due to Product contains glass KENILWORTH, N.J., Oct. 19, 2021 – Mer... photo #1

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Recall notice

Bryant Ranch Prepack Methocarbamol 500mg - recalled due to Mislabeling, USA

4 years ago •source fda.gov • details

Company name: Bryant Ranch Prepack
Brand name: Bryant Ranch Prepack
Product recalled: Methocarbamol 500mg
Reason of the recall: Bottles labeled as Methocarbamol 500mg tablets were found to contain Methocarbamol 750mg tablets.
FDA Recall date: October 19, 2021
Recall details: Burbank, CA, Bryant Ranch Prepack is voluntarily recalling… See more

#recall #drugs #unitedstates

Recalls Bryant Ranch Prepack Methocarbamol 500mg - recalled due to Mislabeling Company name: Bryant Ranch Pr... photo #1

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Recall notice

Cook Medical Transseptal Needle and Transseptal Needle Catheter - recalled due to Complaints of rust on the products, USA

4 years ago •source fda.gov • details

Company name: Cook Medical
Brand name: Cook Medical
Product recalled: Transseptal Needle and Transseptal Needle Catheter
Reason of the recall: Complaints of rust on the products
FDA Recall date: October 19, 2021
Recall details: Bloomington, Ind. — On October 8, 2021, Cook Medical issued a global, voluntary… See more

#recall #medicaldevices #unitedstates

Recalls Cook Medical Transseptal Needle and Transseptal Needle Catheter - recalled due to Complaints of rust... photo #1

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Recall notice

Emergen-C Energy Release & Immunity Support - recalled due to unauthorized pesticide, Ireland

4 years ago •source fsai.ie • details

The FSAI announced the recall of certain batches of Emergen-C Energy Release and Immunity Support Food Supplement due to the presence of the unauthorized pesticide ethylene oxide. Ethylene oxide is a pesticide that is not permitted for use in foods sold in the EU but is approved… See more

#vitamins #recall #ireland #orange

Recalls Emergen-C Energy Release & Immunity Support - recalled due to unauthorized pesticide The FSAI announ... photo #1

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Recall notice

Lupin Irbesartan and Hydrochlorothiazide Tablets - recalled due to of N-nitrosoirbesartan impurity, USA

4 years ago •source fda.gov • details

Company name: Lupin Pharmaceuticals, Inc.
Brand name: Lupin
Product recalled: Irbesartan and Hydrochlorothiazide Tablets USP, 150mg/12.5 mg and 300mg/12.5 mg
Reason of the recall: API batches above the specification limit for the impurity, N-nitrosoirbesartan
FDA Recall date: October 14, 2021
Recall details: Baltimore, Maryland, October 14, 2021:… See more

#blood #recall #drugs #unitedstates