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Safety Reports: Recall

Updated:

Real Time Reports

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
  Comments Comment

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
4   Comments Comment

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
5   Comments Comment

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
4   Comments Comment

Recall notice

Bionpharma Atovaquone Oral Suspension - recalled due to Cohnella bacteria, United States

1 year ago •source fda.gov • details

Bionpharma Inc. is voluntarily recalling (1) a single batch of Atovaquone Oral Suspension at the consumer level. The product was found to be contaminated with Cohnella bacteria. The affected batch of product was manufactured at CoreRx, Inc. and shipped nationwide to customers between December 21, 2023, and… See more

#drugs #recall #unitedstates

Recalls Bionpharma Atovaquone Oral Suspension - recalled due to Cohnella bacteria Bionpharma Inc. is volunta... photo #1
4   Comments Comment

Recall notice

Dynacare Baby Powder - recalled due to potential metal or chemical contaminant, USA

1 year ago •source fda.gov • details

Dynarex Corporation is recalling Dynacare Baby Powder because it has the potential to be contaminated with asbestos. The product was sent to distributors on or after March 11, 2024, by direct delivery in the following states: AL, AR, CO, IL, KY, NC, NJ, PA, TN, FL, WA,… See more

#recall #cosmetics #unitedstates

Recalls Dynacare Baby Powder - recalled due to potential metal or chemical contaminant Dynarex Corporation... photo #1
4   Comments Comment

Recall notice

Bestway Spa pumps recalled due to product overheating, United States

1 year ago •source cpsc.gov • details

The U.S. Consumer Product Safety Commission and Bestway (Hong Kong) International Ltd. have announced the recall of approximately 866,000 AirJet and HydroJet Spa Pumps because the product can overheat causing the plastic housing to ignite, posing a fire hazard. The recalled spa pumps were sold together with… See more

#recall #unitedstates

Recalls Bestway Spa pumps recalled due to product overheating The U.S. Consumer Product Safety Commission an... photo #1
4   Comments Comment

Recall notice

Breas Vivo 45 LS Ventilator - recalled due to formaldehyde exposure, USA

1 year ago •source fda.gov • details

Breas Medical initiated a U.S. nationwide correction of 8,186 Vivo 45 LS ventilator devices. Internal testing of the ventilator identified the potential for short term elevated levels of formaldehyde exposure to users under specific conditions.

Short term formaldehyde emissions may lead to adverse pulmonary or neurological effects… See more

#recall #medicaldevices #unitedstates

Recalls Breas Vivo 45 LS Ventilator - recalled due to formaldehyde exposure Breas Medical initiated a U.S. n... photo #1
312   Comments Comment

Recall notice

B. Braun 0.9% Sodium Chloride for Injection - recalled due to particulate matter and fluid leakage, USA

1 year ago •source fda.gov • details

B. Braun Medical Inc. (B. Braun), is voluntarily recalling two (2) lots of 0.9% Sodium Chloride for Injection USP 1000 mL in E3 containers. The voluntary recall has been initiated due to the potential for particulate matter and fluid leakage of the respective containers. The product was… See more

#recall #drugs #unitedstates

Recalls B. Braun 0.9% Sodium Chloride for Injection - recalled due to particulate matter and fluid leakage B... photo #1
312   Comments Comment

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