Granules Pharma Metformin Hydrochloride Recall [US]

Granules Pharma Metformin Hydrochloride Recall [US]

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US FlagUS/Silver Spring: Granules Pharmaceuticals, Inc., a Chantilly, Virginia establishment, recalls twelve (12) batch/lots of Metformin Hydrochloride Extended-Release Tablets USP, 750 mg from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable FDA levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/dXLm30qX5hG

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/granules-pharmaceuticals-inc-issues-voluntary-nationwide-recall-metformin-hydrochloride-extended

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

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Norpac Fisheries Fresh Shrimp Poke Fish Recall [US]

Norpac Fisheries Fresh Shrimp Poke Fish Recall [US]

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US FlagUS/Silver Spring: Norpac Fisheries Export, a Honolulu, Hawaii establishment, recalls all batch/lots of Fresh Shrimp Poke Fish from the American marketplace and known to have been distributed in the Hawaiian Islands between May 11, 2020 and June 25, 2020 due to suspected risk of Listeria monocytogenes contamination and consequential risk of Gram-positive bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/h3kH30qW1fb

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/norpac-fisheries-export-recalls-shrimp-poke-due-possible-health-risk

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

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Garland Ventures Five Cheese Pasta Shell Recall [US]

Garland Ventures Five Cheese Stuffed Ricotta Shell Recall [US]

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US FlagUS/Silver Spring: Garland Ventures Ltd., a Garland, Texas, establishment, recalls an estimated 1095 cases of Five Cheese Stuffed Ricotta Pasta Shells from the American marketplace due to suspected risk of Listeria monocytogenes contamination and consequential risk of Gram-positive bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/oJWg30qVGMw

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/garland-ventures-ltd-voluntary-recalls-five-cheese-stuffed-shells-because-possible-health-risk

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

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TTDeye Contact Lens Recall [US]

TTDeye Contact Lens Recall [US]

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US FlagUS/Silver Spring: Chengdu Ai Qin E-commerce Co., Ltd. recalls an estimated 1362 pairs of TTDeye branded Colored Contact Lenses from the American marketplace due to suspected failure to gain FDA mandatory pre-sale safety approvals and risk of eye damage and/or blindness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/IOr530qUB5Y

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/chengdu-ai-qin-e-commerce-co-ltd-issues-nationwide-recall-ttdeye-brand-colored-contact-lenses

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

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GSK Children’s Dimetapp & Robitussin Recall [US]

GSK Dimetapp & Robitussin Recall [US]

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US FlagUS/Silver Spring: GSK Consumer Healthcare, a Warren, New Jersey establishment, recalls two batch/lots of Children’s Robitussin Honey Cough and Chest Congestion DM and one lot of Children’s Dimetapp Cold and Cough from the American marketplace due to suspected inclusion of incorrect dosing cups and consequential risks of medication overdose and/or medication under-dosage, all serious health hazards.

FDA: http://ht.ly/bC3e30qRUAQ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gsk-consumer-healthcare-issues-voluntary-nationwide-recall-childrens-robitussinr-honey-cough-and

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Children’s medications are subject to this recall:

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Now Real Food Raw Macadamia Nut Recall [US]

Now Real Food Raw Macadamia Nut Recall [US]

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US FlagUS/Sliver Spring: Now Health Group, Inc. (“NOW”), a Bloomingdale, Illinois establishment, recalls certain batch/lots of Now branded Real Food Raw Macadamia Nuts from the American marketplace due to suspected risk of Salmonella contamination and consequential risk of Gram-positive bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/rYHg30qQY6f

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/now-health-group-inc-voluntarily-recalls-now-real-food-rraw-macadamia-nuts-because-possible-health

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

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Lupin Pharma Metformin Hydrochloride Tablet Recall [US]

Lupin Pharma Metformin Hydrochloride Tablet Recall [US]

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US FlagUS/Silver Spring: Lupin Pharmaceuticals, Inc., a Baltimore, Maryland establishment, recalls certain batch/lots of Lupin Pharma branded Metformin Hydrochloride Extended Release Tablets from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable FDA levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/GfnZ30qQfdN

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lupin-pharmaceuticals-inc-issues-voluntarily-nationwide-recall-one-lot-metformin-hydrochloride

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

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Xi Zhi Liang Konjac Fruit Jelly Cup Recall [US]

Xi Zhi Liang Konjac Fruit Jelly Cup Recall [US]

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US FlagUS/Silver Spring: Rong Shing Trading NY Inc., a Brooklyn, New York establishment, recalls certain batch/lots of Xi Zhi Liang Fruit Jelly Cups (喜唧郎什果果凍杯) from the American marketplace due to 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/p76030qPzKR

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/rong-shing-trading-ny-inc-brooklyn-ny-recalling-its-211oz-600g-xi-zhi-liang-fruit-jelly-cup

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

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Apotex Metformin Hydrochloride Tablet Recall [US]

Apotex Metformin Hydrochloride Tablet Recall [US]

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US FlagUS/Silver Spring: Apotex Corp., a Toronto, Ontario establishment, recalls certain batch/lots of Apotex Corp branded Metformin Hydrochloride Extended-Release Tablets from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable FDA levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/HmUE30qPhSK

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/apotex-corp-issues-voluntary-nationwide-recall-metformin-hydrochloride-extended-release-tablets

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

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Actavis Pharma Metformin Hydrochloride Tablet Recall [US]

Actavis Pharma Metformin Hydrochloride Tablet Recall [US]

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US FlagUS/Silver Spring: Teva Pharmaceuticals USA, Inc., a Parsippany, New Jersey establishment and subsidiary of Teva Pharmaceutical Industries Ltd. of Petah Tikva, Israel, recalls certain batch/lots of Actavis Pharma, Inc. branded Metformin Hydrochloride Extended Release Tablets from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable FDA levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/q9Pu30qOed1

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teva-pharmaceuticals-usa-inc-initiates-voluntary-nationwide-recall-metformin-hydrochloride-extended

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

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Time-Cap Labs Metformin Hydrochloride Tablet Recall [US]

Time-Cap Labs Metformin Hydrochloride Tablet Recall [US]

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US FlagUS/Silver Spring: Marksans Pharma Limited, a Verna, Goa, India establishment, recalls certain batch/lots of Time-Cap Labs, Inc. branded Metformin Hydrochloride Extended Release Tablets from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable FDA levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/upL630qNRGM

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/marksans-pharma-limited-issues-voluntary-nationwide-recall-metformin-hydrochloride-extended-release

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

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Amneal Metformin Hydrochloride Tablet Recall [US]

Logo - Metformin Hydrochloride Extended Release Tablets

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US FlagUS/Silver Spring: Amneal Pharmaceuticals LLC, a Bridgewater, New Jersey establishment, recalls all current batch/lots of Metformin Hydrochloride Extended Release Tablets from the American marketplace due to suspected N-Nitrosodimethylamine (“NDMA”) contamination in amounts above acceptable FDA levels with consequential risks of Cancer, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/pU8030qNxkW

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/amneal-pharmaceuticals-llc-issues-voluntary-nationwide-recall-metformin-hydrochloride-extended

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

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Biocell Breast Implant & Tissue Expander Recall [US]

US FlagUS/Silver Spring: Logo - Allergan AestheticsAllergan Aesthetics, an Irvine, California establishment and subsidiary of AbbVie of North Chicago, Illinois, recalls an estimated 52,000 Biocell Breast Implants and/or Tissue Expanders from the American marketplace due to suspected risk of Breast Implant Associated Anaplastic Large Cell Lymphoma (“BIA-ALCL”), a type of Non-Hodgkin’s Lymphoma (Cancer of the Immune System) and consequential risk of possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/j7Bw30qN5k9

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/allergan-aesthetics-launches-dedicated-multi-channel-campaign-contact-patients-who-may-not-be-aware

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Breast Implants and/or Tissue Expanders are subject to this recall:

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Wegmans Tuna Salad Recall [US]

US FlagUS/Silver Spring: Logo - Wegmans Food Markets, Inc.Wegmans Food Markets, Inc., a Rochester, New York establishment, recalls certain batch/lots of Wegmans branded Tuna Salads from the American marketplace due to suspected unidentified foreign matter contamination and consequential risk of choking, oral injury, internal ingestion and GI tract laceration damage, all serious health and safety hazards.

Wegmans: http://ht.ly/JKvq30qLHu0

Direct link: https://www.wegmans.com/news-media/product-recalls/wegmans-tuna-salad/

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

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MasterPharm Finasteride Plus Capsule Recall [US]

US FlagUS/Silver Spring: Logo - MasterPharm LLCMasterPharm, LLC., a Garden City, New York establishment, recalls certain batch/lots of Finasteride Plus Capsules from the American marketplace due to suspected undeclared Minoxidil, an Antihypertensive drug, at levels greater than those found in FDA approved products with consequential risks of severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/5EyL30qJ9xm

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/masterpharm-llc-issues-voluntary-nationwide-recall-finasteride-plus-125mg-due-presence-undeclared

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

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