Comercial Mexicana Tropique Fruit Jelly Cup Recall [US]

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US/Silver Spring: Comercial Mexicana International Inc., a Bethpage New York establishment, recalls certain batch/lots of Tropique Fruit Jelly Cup Confectionery products from the American marketplace due to the presence of Seaweed Extract, specifically Carrageenan, and consequential risks of choking, oral injury, internal ingestion, GI tract laceration damage and bowel obstruction, all serious health and safety hazards.

FDA: http://ht.ly/1FWL30rgyRI

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/comercial-mexicana-international-inc-recalls-tropique-assorted-fruit-jelly-bag-309pcs1006oz-and

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Jelly Cup products are subject to this recall:

Hadson Toko Eishindo Mini Cup Jelly Recall [US]

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US/Silver Spring: Hadson Toko Trading Co., Inc., a Maspeth, New York establishment, recalls certain batch/lots of Eishindo Mini Cup Jelly from the American marketplace due to the suspected presence of Konjac Powder and consequential risk of choking, asphyxiation, oral injury, internal ingestion and GI tract laceration damage, all serious health and safety hazards.

FDA: http://ht.ly/o96w30rfa43

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hadson-toko-trading-co-inc-recalls-eishindo-mini-cup-jelly-50pcs-because-potential-choking-hazard

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Fruit Jelly Cup products are subject to this recall:

Cost Plus, Great Value & Full Circle Parsley Recall [US]

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US/Silver Spring: Red Monkey Foods, a Springfield, Missouri establishment, recalls certain batch/lots of Organic Parsley Spice products from the American marketplace due to suspected Salmonella contamination and consequential risks of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/w0CQ30reZnr

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/red-monkey-foods-inc-recalls-parsley-and-herbes-de-provence-because-possible-health-risk

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Organic Parsley Spice products are subject to this recall:

Sauer Brands Spice Hunter Dried Spice Recall [US]

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US/Silver Spring: Sauer Brands, Inc., a Richmond, Virginia establishment, recalls certain batch/lots of numerous Spice Hunter branded Dried Spices from the American marketplace due to suspected Salmonella contamination and consequential risks of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/UeRr30reOpw

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sauer-brands-inc-voluntarily-recalls-certain-spice-hunter-products-because-potential-salmonella

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Bottled Dried Spices are subject to this recall:

Meijer Fresh Cantaloupe & Fruit Salad Recall [US]

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US/Silver Spring: Meijer Inc., a Walker, Michigan establishment, in conjunction with Eagle Produce, LLC, of Aguila, Arizona, recalls certain batch/lots of Whole Cantaloupes and certain Fruit Salads made with Cut Cantaloupe pieces from the American marketplace due to suspected Salmonella contamination and consequential risks of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/kjAK30re0Xq

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/meijer-recalls-whole-cantaloupes-and-select-cut-cantaloupe-trays-due-potential-health-risk

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Fresh Cantaloupes and Fruit Salads containing Cantaloupe are subject to this recall (in alphabetical order):

Seneca & Clancy’s Cinnamon Apple Chip Recall [US]

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US/Silver Spring: Seneca Snack Company, a Marion, New York establishment, recalls certain batch/lots of Seneca branded Cinnamon Apple Chips and Clancy’s branded Cinnamon Apple Chips from the American marketplace due to suspected Salmonella contamination and consequential risks of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/L8Xk30rdrEG

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/seneca-recalls-cinnamon-apple-chips-because-possible-health-risk

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Apple Chip Snack Food products are subject to this recall:

Walmart Cut Fruit & Fruit Salad Recall [US]

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US/Silver Spring: Country Fresh, LLC, a Grand Rapids, Michigan establishment, recalls certain batch/lots of Walmart branded Cut Fruit and Fruit Salads from the American marketplace due to possible Listeria monocytogenes contamination and consequential risks of Gram-positive bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/wdAL30rdgFg

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/country-fresh-expands-voluntary-recall

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Cut Fruit and Fruit Salads are subject to this recall (in alphabetical order):

Barbie, Hot Wheels & PAW Patrol Hand Sanitizer Recall [US]

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US/Silver Spring: Ashtel Studios, an Ontario, California establishment, recalls certain batch/lots of Children’s Character Licensed Hand Sanitizer products from the American marketplace due to reported resemblance to Children’s Food or Drink Containers and consequential risks of child poisoning, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/cG2y30rd7KO

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ashtel-studios-issues-voluntary-recall-licensed-hand-sanitizers-packaged-084-fluid-ounce-pouches-due

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Hand Sanitizer products are subject to this recall:

Walmart & RaceTrac Cut Watermelon and Salad Recall [US]

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US/Silver Spring: Country Fresh, LLC, a Grand Rapids, Michigan establishment, recalls certain batch/lots of Walmart branded, Country Fresh branded and RaceTrac branded Cut Watermelon Chunks and Fruit Salads made with Cut Watermelon Chunks from the American marketplace due to possible Listeria monocytogenes contamination and consequential risks of Gram-positive bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/WCwZ30rd1gi

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/country-fresh-voluntary-product-recall

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Watermelon Chunks and Fruit Salads are subject to this recall:

DMM VISSION Cleaner branded Hand Sanitizer Recall [US]

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US/Silver Spring: DMM VISSION SA de CV, an Estado de México, México establishment, recalls at least five (5) batch/lots of Cleaner branded Hand Sanitizer from the American marketplace due to possible Methanol contamination (also called Methyl Alcohol or “Wood Alcohol”) from the American marketplace due to risks of poisoning, oral injury, internal ingestion, GI tract laceration damage, blindness and death, all serious health and safety hazards requiring immediate medical intervention.

FDA: http://ht.ly/XsbW30rcQ9x

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dmm-vission-sa-de-cv-issues-voluntary-nationwide-recall-cleaner-hand-sanitizer-500-ml-and-1200-ml

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Hand Sanitizer products are subject to this recall:

Thomson Intl. Red, Yellow, White Onion Recall [US]

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US/Sliver Spring: Thomson International Inc., a Bakersfield, California establishment, recalls certain batch/lots of Red, Yellow, White and Sweet Yellow Fresh Onions from the American marketplace due to suspected Salmonella Newport contamination and consequential risk of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/GVh830rcBus

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/thomson-international-inc-conducts-voluntary-recall-red-yellow-white-and-sweet-yellow-onions-because

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Fresh Onions are subject to this recall:

M branded Hand Sanitizer Alcohol Antiseptic Recall [US]

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US/Silver Spring: Medek, LLC, an Alamo, Texas establishment, recalls all current batch/lots of M branded Hand Sanitizer Alcohol Antiseptic 80% from the American marketplace due to possible Methanol contamination (also called Methyl Alcohol or “Wood Alcohol”) from the American marketplace due to risks of poisoning, oral injury, internal ingestion, GI tract laceration damage, blindness and death, all serious health and safety hazards requiring immediate medical intervention.

FDA: http://ht.ly/cBfc30raJ7f

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/medek-llc-issues-voluntary-nationwide-recall-m-hand-sanitizer-due-potential-presence-methanol-wood

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Hand Sanitizer products are subject to this recall:

BD Alaris Infusion Pump System Recall [US]

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US/Silver Spring: Becton, Dickinson and Company (“BDC”), a Franklin Lakes, New Jersey establishment, updates its existing recall for various models of BD Alaris Infusion Pump Systems from the American marketplace after an upgrading and reclassification of the original notification published by the US Food and Drug Administration (“FDA”) to Class I, the most serious and potentially deadly classification of medical device recall.

The original recall was initiated due to possible operational failure and consequential inaccurate dosage, failure to dose and possible life-changing complications including death, all serious health and safety hazards.

FDA: http://ht.ly/Irmt30r8C9r

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-provides-update-previously-disclosed-recall-bd-alaris-system-hardware

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Infusion Pump Systems are subject to this recall:

Leafree Instant Hand Sanitizer Recall [US]

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US/Silver Spring: CorgioMed, LLC, a Gaithersburg, Maryland establishment, recalls all current batch/lots of Leafree Instant Hand Sanitizer-Aloe Vera from the American marketplace due to reported labelling as “EDIBLE ALCOHOL” and consequential risks of inadvertent alcohol poisoning, alcohol toxicity and GI tract laceration damage, all serious health and safety hazards.

FDA: http://ht.ly/466S30r8mCQ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/corgiomed-llc-issues-voluntary-nationwide-recall-all-lots-leafree-instant-hand-sanitizer-aloe-vera

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Leafree Instant Hand Sanitizer products are subject to this recall:

bio aaa Advance Hand Sanitizer Recall [US]

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US/Silver Spring: AJR Trading LLC, a Tlalnepantia, Mexico establishment, recalls an estimated 2,004 units of bio aaa branded Advance Hand Sanitizer from the American marketplace due to possible Methanol contamination (also called Methyl Alcohol or “Wood Alcohol”) from the American marketplace due to risks of poisoning, oral injury, internal ingestion, GI tract laceration damage, blindness and death, all serious health and safety hazards requiring immediate medical intervention.

FDA: http://ht.ly/JHhL30r8hJo

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ajr-trading-llc-issues-voluntary-nationwide-recall-bio-aaa-advance-hand-sanitizer-480-ml-bottles-lot

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Hand Sanitizer products are subject to this recall: