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Safety Reports: Recall

Updated: November 5, 2024 3:01 PM

Real Time Reports

Recall notice

Boulla ZoomMax and ZapMax Capsules - recalled due to Sildenafil and Diclofenac, USA

1 year ago •source fda.gov • details

Boulla LLC is voluntarily recalling ZoomMax and ZapMax Capsules to the consumer level. The products were found to be tainted with sildenafil and diclofenac. Products containing sildenafil and diclofenac cannot be marketed as dietary supplements. ZoomMax and ZapMax capsules are unapproved new drugs for which safety and… See more

#vitamins #recall #amazon #unitedstates

Recalls Boulla ZoomMax and ZapMax Capsules - recalled due to Sildenafil and Diclofenac Boulla LLC is volunta... photo #1

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Recall notice

Aqua Mix - Grout Deep Clean recalled due to lack of child-resistant packaging, Canada

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

Custom Building Products Of Canada Ltd recalled their Aqua Mix - Grout Deep Clean due to its lack of child-resistant packaging which is capable of causing burns to eyes or skin,. The product was distributed across Canada.

The lack of child-resistant packaging could lead to unintentional exposure… See more

#recall #canada

Recalls Aqua Mix - Grout Deep Clean recalled due to lack of child-resistant packaging Custom Building Produc... photo #1

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Recall notice

Dynarex Corporation Baby Powder - recalled due to Potential Metal or Chemical Contaminant, USA

1 year ago •source fda.gov • details

Dynarex Corporation is expanding the recall initiated on September 19, 2024, to include an additional 373 cases of item number 4875, Dynacare Baby Powder, 14 oz., as well as 647 cases of item number 4874, Dynacare Baby Powder, 4 oz., because they have the potential to be… See more

#recall #unitedstates

Recalls Dynarex Corporation Baby Powder - recalled due to Potential Metal or Chemical Contaminant Dynarex C... photo #1

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Recall notice

Medtronic MiniMed series insulin pumps - recalled due to Defect, USA

1 year ago •source fda.gov • details

Medtronic plc voluntarily issued a field action starting on July 31, 2024, notifying global customers of its MiniMed™ 600 series or 700 series insulin pumps to follow their pump’s built-in alerts and alarms for battery status and to contact Medtronic if they observe changes in the battery… See more

#ketogummiesscam #scam #recall #medicaldevices #unitedstates

Recalls Medtronic MiniMed series insulin pumps - recalled due to Defect Medtronic plc voluntarily issued a f... photo #1

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Recall notice

Gorilla Mind Rauwolscine Dietary Supplement recalled due to Salmonella, USA

1 year ago •source accessdata.fda.gov • details

Gorilla Mind LLC has voluntarily initiated a recall of its Rauwolscine Dietary Supplement due to potential Salmonella contamination. The product has been distributed nationwide.

The product recalled is the Gorilla Mind Rauwolscine Dietary Supplement, marketed for appetite suppression, increased fat loss, and energy. Each bottle contains 90… See more

#vitamins #recall #unitedstates

Recalls Gorilla Mind Rauwolscine Dietary Supplement recalled due to Salmonella Gorilla Mind LLC has voluntar... photo #1

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Recall notice

AK Forte Dietary Supplement - recalled due to unapproved drug, USA

1 year ago •source fda.gov • details

C&A Naturistics is voluntarily recalling all lots of AK Forte, 400 mg tablets, to the consumer level. FDA analysis has found the product to be tainted Diclofenac, Dexamethasone, and Methocarbamol. Products containing diclofenac, dexamethasone, and methocarbamol cannot be marketed as dietary supplements. AK Forte tablets is an… See more

#recall #drugs #unitedstates

Recalls AK Forte Dietary Supplement - recalled due to unapproved drug C&A Naturistics is voluntarily recalli... photo #1

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Recall notice

Staska Pharmaceuticals Ascorbic Acid Solution - recalled due to glass particulates, USA

1 year ago •source fda.gov • details

Staska Pharmaceuticals, INC. is voluntarily recalling 1 lot of Ascorbic Acid Solution for Injection to the user level. This is due to the presence of glass particulates in one lot of vials used in the production of this batch. The product was distributed nationwide in USA to… See more

#recall #drugs #unitedstates

Recalls Staska Pharmaceuticals Ascorbic Acid Solution - recalled due to glass particulates Staska Pharmaceut... photo #1

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Recall notice

Philips Respironics Trilogy Evo Ventilators- recalled due to inaccurate flow measurements, USA

1 year ago •source fda.gov • details

Philips Respironics issued a voluntary recall for Trilogy Evo Ventilators regarding the use of in-line nebulizers. The products have been distributed nationwide.

Potential hazards to patients from these conditions may include respiratory discomfort; lung injury from too much air in the lungs or change in pressure (volutrauma/barotrauma);… See more

#recall #medicaldevices #unitedstates

Recalls Philips Respironics Trilogy Evo Ventilators- recalled due to inaccurate flow measurements Philips Re... photo #1

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Outbreak

Health Alert for Darwin's Natural Selections Pet Food due to Salmonella and Listeria, United States

1 year ago •source fda.gov • details

The U.S. Food and Drug Administration (FDA) has issued a warning to pet owners about certain lots of Darwin's Natural Selections Pet Food due to contamination with Salmonella and Listeria monocytogenes. The affected products are sold in frozen 2-pound packages and are generally distributed online through a… See more

#recall #petfood #unitedstates

Outbreak Health Alert for Darwin’s Natural Selections Pet Food due to Salmonella and Listeria The U.S. Food a... photo #1

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Recall notice

Gilead Veklury (remdesivir) for Injection - recalled due to presence of Glass Particle, USA

1 year ago •source fda.gov • details

Gilead Sciences, Inc. issued a voluntary recall of one lot of Veklury® (remdesivir) for Injection to the consumer level. The product was distributed nationwide in the United States, beginning 16 July 2024

Risk Statement: The administration of an injectable product that contains glass particles may result in… See more

#recall #drugs #unitedstates

Recalls Gilead Veklury (remdesivir) for Injection - recalled due to presence of Glass Particle Gilead Scienc... photo #1

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Safety Reports: Recall

Real Time Reports

Boulla ZoomMax and ZapMax Capsules - recalled due to Sildenafil and Diclofenac, USA

Aqua Mix - Grout Deep Clean recalled due to lack of child-resistant packaging, Canada

Dynarex Corporation Baby Powder - recalled due to Potential Metal or Chemical Contaminant, USA

Medtronic MiniMed series insulin pumps - recalled due to Defect, USA

Gorilla Mind Rauwolscine Dietary Supplement recalled due to Salmonella, USA

AK Forte Dietary Supplement - recalled due to unapproved drug, USA

Staska Pharmaceuticals Ascorbic Acid Solution - recalled due to glass particulates, USA

Philips Respironics Trilogy Evo Ventilators- recalled due to inaccurate flow measurements, USA

Health Alert for Darwin's Natural Selections Pet Food due to Salmonella and Listeria, United States

Gilead Veklury (remdesivir) for Injection - recalled due to presence of Glass Particle, USA

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