Applaws, AVA & by Sainsbury’s Cat Food Recall Update [UK]

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UK/London: Fold Hill Foods, a Boston, Lincolnshire, England establishment, updates its existing recall for certain batch/lots of Applaws, AVA and by Sainsbury’s Cat Food products from the British marketplace to include all best-before dates for Applaws products with the site code GB218E5009.

The original recall notification was initiated due to suspected Pancytopenia infection and consequential risks of Anemia (low levels of red blood cells), Leukopenia (low levels of white blood cells and/or Thrombocytopenia (low platelet levels), all serious health and safety situations requiring immediate veterinary intervention.

FSA: http://ht.ly/7qMp30rN5Iq

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-36-2021-update-1

Additional information:
The UK Food Standards Agency (“FSA”) reports the following Cat Food products are subject to recall:

Applaws, AVA & by Sainsbury’s Cat Food Recall [UK]

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UK/London: Fold Hill Foods, a Boston, Lincolnshire, England establishment, recalls certain batch/lots of Applaws, AVA and by Sainsbury’s Cat Food products from the British marketplace due to suspected Pancytopenia infection and consequential risks of Anemia (low levels of red blood cells), Leukopenia (low levels of white blood cells and/or Thrombocytopenia (low platelet levels), all serious health and safety situations requiring immediate veterinary intervention.

FSA: http://ht.ly/LSHr30rMcXX

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-36-2021

Additional information:
The UK Food Standards Agency (“FSA”) reports the following Cat Food products are subject to recall:

LifeSeasons Blood Nourish-R Supplement Recall [US]

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US/Washington: LifeSeasons Inc., a Springville, Utah establishment, recalls an estimated 7,800 bottles of LifeSeasons Blood Nourish-R Supplements from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/I2l030rLH8e

Direct link: https://www.cpsc.gov/Recalls/2021/UST-Recalls-Bottles-of-LifeSeasons-Blood-Nourish-R-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain LifeSeasons Blood Nourish-R Supplements marketed, sold and delivered in the United States, as follows:

Puricia Hand Sanitizer Recall [Canada]

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Canada/Ottawa: Pharmaberg Inc., a Delta, British Columbia establishment, recalls certain batch/lots of Puricia Hand Sanitizer products from the Canadian marketplace due to reported undeclared impurities as well as Benzene and Methanol contamination at elevated levels with consequential risks of operational ineffectiveness, failure to prevent microbial spread and possible bacterial and/or viral contamination, all serious health and safety hazards.

HCSC: http://ht.ly/cOx430rLD7t

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75845r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Hand Sanitizer products are subject to this recall:

Living Free Dietary Supplement Recall [US]

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US/Silver Spring: Bea Lydecker’s Naturals, Inc. an Oregon City, Oregon establishment, recalls certain batch/lots of six (6) Living Free branded Dietary Supplement drug products from the American marketplace due to improperly declared Soy Lecithin, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

FDA: http://ht.ly/prKp30rLAx8

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bea-lydeckers-naturals-inc-issues-allergy-alert-undeclared-soy-lecithin-living-free-dietary

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

Philips PAP, CPAP & Mechanical Ventilator Recall [US]

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US/Silver Spring: Royal Philips, an Amsterdam, Netherlands establishment, recalls certain batch/lots of various Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (“CPAP”) and other Mechanical Ventilator Devices from the American marketplace to address identified potential health risks related to the Polyester-based Polyurethane (“PE-PUR”) Sound Abatement Foam component in these devices, a serious health and safety hazard requiring medical intervention.

FDA: http://ht.ly/hMkQ30rL0GE

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/philips-issues-recall-notification-mitigate-potential-health-risks-related-sound-abatement-foam

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Bi-Level PAP, CPAP and Ventilators are subject to this recall:

SynerClear Nutritional Supplement Recall [Canada]

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Canada/Ottawa: Naturo Aid Pharmaceutical Inc., a Maple Ridge, British Columbia establishment, recalls numerous batch/lots of SynerClear Nutritional Supplement products from the Canadian marketplace due to undeclared Milk, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

HCSC: http://ht.ly/qwrD30rJm9g

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75711r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Nutritional Supplement products are subject to this recall:

Protat Sea Salt Piercing Aftercare Spray Recall [Australia]

Australia/Canberra: Protat Pty Ltd., a Brompton, South Australia establishment, recalls certain batch/lots of Protat Natural Sea Salt Plus Tea Tree Hygienic Body Piercing Aftercare Spray from the Australian marketplace due to suspected Pseudomonas aeruginosa contamination and consequential risks of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

ACCC: http://ht.ly/uD1430rJsr3

Direct link: https://www.productsafety.gov.au/recall/protat-pty-ltd-protat-natural-sea-salt-plus-tea-tree-hygienic-body-piercing-aftercare-spray-50ml

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following medications are subject to this recall:

DermOtic Oil Ear Drops Recall [Canada]

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Canada/Ottawa: Hill Dermaceuticals Inc., a Mississauga, Ontario establishment, recalls numerous batch/lots of DermOtic Oil Ear Drops from the Canadian marketplace due to suspected Glass Fragment Contamination and consequential risks of outer ear injury, tympanic membrane laceration, infection hearing damage, all serious health and safety hazards.

HCSC: http://ht.ly/WmHi30rJf7L

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75709r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Ear Drops are subject to this recall:

MSIKU White Wedding Dried Cannabis Recall [Canada]

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Canada/Ottawa: AtlantiCann Medical Inc., a Sackville, Nova Scotia establishment, recalls an estimated 4176 units of MSIKU White Wedding Dried Cannabis products from the Canadian marketplace due to suspected incorrect THC values with consequential risks of underdose, failure to relieve pain and/or nausea and possible compensatory overdose, all serious health and safety hazards.

HCSC: http://ht.ly/jQx230rILW5

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75609r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Cannabis products are subject to this recall:

Medically Minded Hand Sanitizer Recall [US]

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US/Silver Spring: Global Sanitizers, a Las Vegas, Nevada establishment, recalls an estimated 50,000 bottles of Medically Minded branded Hand Sanitizer products 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/P1Ga30rIfu4

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/global-sanitizers-issues-voluntary-nationwide-recall-medically-minded-hand-sanitizer-due-presence

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

Supercheap Auto CA Reclining Lounger Chair Recall [Australia]

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Australia/Canberra: Supercheap Auto Pty Ltd, a Strathpine, Queensland establishment, recalls certain batch/lots of CA Reclining Lounger Chairs from the Australian marketplace due to reported possible structural collapse and consequential risks of falls, laceration, bone fracture and concussion, all serious safety hazards.

ACCC: http://ht.ly/Deq830rHCxA

Direct link: https://www.productsafety.gov.au/recall/supercheap-auto-pty-ltd-sca-reclining-lounger-chair

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following Lounger Chairs are subject to this recall:

Welmate Lidocaine Numbing Cream Recall [US]

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US/Washington: YYBA Corp., doing business as Wellspring, a Monsey, New York establishment, recalls an estimated 15,000 jars of Welmate Lidocaine Numbing Cream from the American marketplace due to failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/DH9A30rGou9

Direct link: https://www.cpsc.gov/Recalls/2021/YYBA-Recalls-Welmate-Lidocaine-Numbing-Cream-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves Welmate Lidocaine Numbing Cream marketed, sold and delivered in the United States, as follows:

Nuri Shogun-X 7000, 69MODE & Thumbs Up 7 Supplements

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US/Silver Spring: Nuri Trading, a Newton, New Jersey, establishment, recalls all current batch/lots of Shogun-X 7000 Supplement Capsules, 69MODE Blue 69 Supplement Capsules, Thumbs Up 7 (Black) 25K Supplement Capsules and Thumbs Up 7 (White) 11K Supplement Capsules from the American marketplace due to reported undeclared Sildenafil, Tadalafil and Vardenafil, three (3) FDA approved drugs for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/4jiJ30rDJ1l

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nuri-trading-llc-issues-voluntary-nationwide-recall-shogun-x-7000-thumbs-7-black-25k-thumbs-7-white

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

Ummzy Krazy Night, Shogun-X & Thumbs Up Recall [US]

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US/Silver Spring: Ummzy LLC, a Palisades Park, New Jersey establishment, recalls all current batch/lots of Krazy Night Dietary Supplement Capsules, Shogun-X 15000 mg Dietary Supplement Capsules and Thumbs Up 7 Red 70K Dietary Supplement Capsules from the American marketplace due to reported undeclared Sildenafil, Tadalafil and Vardenafil, three (3) FDA approved drugs for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/TkLw30rDCMy

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ummzy-llc-issues-voluntary-nationwide-recall-thumbs-7-red-70k-shogun-x-15000mg-and-krazy-night-due

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