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Safety Reports: Recall

Updated: October 7, 2024 4:03 PM

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

1 month ago •source fda.gov • details

Recall notice

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

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

1 month ago •source fda.gov • details

Outbreak

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 #salmonella

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

1 month ago •source fda.gov • details

Recall notice

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

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

2 months ago •source fda.gov • details

Recall notice

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 our customers between December 21, 2023,… See more

#drugs #recall #unitedstates

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

2 months ago •source fda.gov • details

Recall notice

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

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Bestway Spa pumps recalled due to product overheating, United States

2 months ago •source cpsc.gov • details

Recall notice

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

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

3 months ago •source fda.gov • details

Recall notice

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

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

3 months ago •source fda.gov • details

Recall notice

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

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Baxter Heparin Sodium Chloride Injection - recalled due to elevated endotoxin levels, USA

3 months ago •source fda.gov • details

Recall notice

Baxter International Inc. is voluntarily recalling one lot of Heparin Sodium in 0.9% Sodium Chloride Injection to the consumer level due to the potential for elevated endotoxin levels based on issues related to the bacterial endotoxin test specific to lot number. This issue affects one lot of… See more

#recall #drugs #unitedstates

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Abbott FreeStyle Libre® 3 sensors - recalled due to Sensors incorrect readings, USA

3 months ago •source fda.gov • details

Recall notice

Abbott has initiated a voluntary medical device correction for a small number of FreeStyle Libre® 3 sensors due to sensors may provide incorrect high glucose readings. The product was distributed in the United States during the first half of May 2024.

The FreeStyle Libre 3 system includes… See more

#recall #medicaldevices #unitedstates

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Safety Reports: Recall

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

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

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

Bestway Spa pumps recalled due to product overheating, United States

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

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

Baxter Heparin Sodium Chloride Injection - recalled due to elevated endotoxin levels, USA

Abbott FreeStyle Libre® 3 sensors - recalled due to Sensors incorrect readings, USA

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