Vyaire Medical Issues Voluntary Correction for Certain bellavista™ Ventilators in Specific Software Configurations

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In December 2021, imtmedical ag, a subsidiary of Vyaire Medical, initiated a voluntary field correction for certain bellavista™ ventilators. With specific software version and configuration combinations, the ventilators can cease ventilation and generate a technical failure alarm 305. There is a pot

Source: Food and Drugs Administration--Recalls/Safety Alerts

Vyaire Medical Issues Voluntary Correction for Certain bellavista™ Ventilators in Specific Software Configurations

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In December 2021, imtmedical ag, a subsidiary of Vyaire Medical, initiated a voluntary field correction for certain bellavista™ ventilators. With specific software version and configuration combinations, the ventilators can cease ventilation and generate a technical failure alarm 305. There is a pot

Source: Food and Drugs Administration--Recalls/Safety Alerts

Junp LLC Issues Voluntary Nationwide Recall of MegMan Performance Booster Capsules Due to the Presence of Tadalafil

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Brooklyn, NY Junp LLC is voluntarily recalling Lot number 2010291, Exp Date: 01/07/2024 of MegMan Performance Booster capsules, packaged in 10-count blisters packaged in a carton to the consumer level. Junp LLC was notified by Amazon that laboratory analysis has found the product to be tainted wit

Source: Food and Drugs Administration--Recalls/Safety Alerts

Junp LLC Issues Voluntary Nationwide Recall of MegMan Performance Booster Capsules Due to the Presence of Tadalafil

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Brooklyn, NY Junp LLC is voluntarily recalling Lot number 2010291, Exp Date: 01/07/2024 of MegMan Performance Booster capsules, packaged in 10-count blisters packaged in a carton to the consumer level. Junp LLC was notified by Amazon that laboratory analysis has found the product to be tainted wit

Source: Food and Drugs Administration--Recalls/Safety Alerts

Golden Medal Mushroom Inc. Recalls Enoki Mushrooms Because of Possible Health Risk

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Golden Medal Mushroom Inc. of Los Angeles, CA is recalling all cases of its 200g/7.05-ounce packages of Enoki Mushrooms, lot # 300511, product of China, because it has the potential to be contaminated with Listeria monocytogenes

Source: Food and Drugs Administration--Recalls/Safety Alerts

El Super Leon Ponchin Snacks Inc Recalls Saladitos Dry Salted Plums Because of Possible Health Risk

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El Super Leon Ponchin Snacks Inc of San Diego, CA (February 3rd, 2022) is recalling Saladitos Dry Salted Plums with and without Chili, El Leoncito and El Super Leon brands, because it has the potential to be contaminated with lead.

Source: FDA Food Safety Recalls RSS Feed

El Chavito, Inc. Recalls Saladitos Dried Salted Plums and Saladitos Enchilados Salted Plums with Chili Because of Possible Health Risk

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EL CHAVITO, INC. of San Diego, CA is recalling all lots of Saladitos Dried Salted Plums and Saladitos Enchilados Salted Plums With Chili because it has the potential to be contaminated with lead.

Source: FDA Food Safety Recalls RSS Feed

A&E Corrales LLC Recalls Saladitos Dried Salted Plums with Chili Because of Possible Health Risk

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A&E Corrales LLC, Seattle, WA is recalling Saladitos Dried Salted Plums With Chili because it has the potential to be contaminated with lead. Lead is a toxic substance present in our environment in small amounts and everyone is exposed to some lead from daily actions such as inhaling dust, eating

Source: FDA Food Safety Recalls RSS Feed

SD BIOSENSOR, Issues Notification of Voluntary Recall of ‘STANDARD Q COVID-19 Ag Home Test’

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Biosensor, Inc., a global in-vitro diagnostics company, is voluntarily recalling its STANDARD Q COVID-19 Ag Home Test in the United States, due to confirmed reports that the test kits were illegally imported into the United States. The STANDARD Q COVID-19 Ag Home Test is not authorized, cleared or a

Source: Food and Drugs Administration--Recalls/Safety Alerts

SD BIOSENSOR, Issues Notification of Voluntary Recall of ‘STANDARD Q COVID-19 Ag Home Test’

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Biosensor, Inc., a global in-vitro diagnostics company, is voluntarily recalling its STANDARD Q COVID-19 Ag Home Test in the United States, due to confirmed reports that the test kits were illegally imported into the United States. The STANDARD Q COVID-19 Ag Home Test is not authorized, cleared or a

Source: Food and Drugs Administration--Recalls/Safety Alerts